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organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 66| Part 5| May 2010| Page o1183
https://doi.org/10.1107/S1600536810014728

Ethyl 5-oxo-2,3-di­phenyl­cyclo­pentane-1-carboxyl­ate

Claude N. Lamb,a* Zerihun Assefaa and Richard E. Sykorab

aNorth Carolina A&T State University, Department of Chemistry, Greensboro, NC 27411, USA, and bUniversity of South Alabama, Department of Chemistry, Mobile, AL 36688-0002, USA
*Correspondence e-mail: clamb@ncat.edu

(Received 3 March 2010; accepted 21 April 2010; online 28 April 2010)

The title compound, C20H20O3, was prepared by an acyl­oin-type condensation reaction in the presence of sodium sand and dry ether using ethyl cinnamate as the starting material. The C—O bond lengths for the carbonyl groups are 1.191 (2) and 1.198 (2) Å, while the C—O bond in the ester group is 1.335 (2) Å. The C—C bond lengths in the phenyl groups average 1.375 Å, while the C—C bonds in the cyclo­penta­none ring average 1.525 Å, indicating single C—C bonds in the latter.

Related literature

For the first synthesis of the title compound, see: Totton et al. (1965[Totton, E. L., Kilpatri, G. R., Horton, N. & Blakeney, S. A. (1965). J. Org. Chem. 30, 1647-1648.]). For general methods of β-keto ester preparation, see: March (1985[March, J. (1985). Advanced Organic Chemistry, 3rd ed. New York: John Wiley and Sons.]); Shiosaki et al.(1981[Shiosaki, K., Fels, G. & Rapoport, H. (1981). J. Org. Chem. 46, 3230-3234.]); Matsumoto et al. (1973[Matsumoto, K., Suzuki, M., Iwasaki, T. & Miyoshi, M. (1973). J. Org. Chem. 38, 2731.]). For acyl­oin-type condensation reactions of α, β unsaturated esters, see: Totton et al. (1961[Totton, E. L., Freeman, R. C., Powell, H. & Yarboro, T. L. (1961). J. Org. Chem. 26, 343-346.], 1965[Totton, E. L., Kilpatri, G. R., Horton, N. & Blakeney, S. A. (1965). J. Org. Chem. 30, 1647-1648.], 1967[Totton, E. L., Camp, N. C., Cooper, G. M., Haywood, B. D. & Lewis, D. P. (1967). J. Org. Chem. 32, 2033-2034.]); Singh & Totton (1981[Singh, P. & Totton, E. L. (1981). Cryst. Struct. Commun. 10, 739-743.]). The mechanism of this condensation reaction was first suggested by Weidlich (1938[Weidlich, H. A. (1938). Berichte, 71, 1601-1603.]) and confirmed by the successful synthesis of several adducts.

[Scheme 1]

Experimental

Crystal data

  • C20H20O3

  • Mr = 308.36

  • Monoclinic, C 2/c

  • a = 27.4961 (13) Å

  • b = 7.4008 (2) Å

  • c = 18.7063 (10) Å

  • β = 115.389 (6)°

  • V = 3439.0 (3) Å3

  • Z = 8

  • Mo Kα radiation

  • μ = 0.08 mm−1

  • T = 295 K

  • 0.14 × 0.14 × 0.08 mm
Data collection

  • Oxford Diffraction Xcalibur Eos diffractometer

  • Absorption correction: analytical [CrysAlis PRO (Oxford Diffraction, 2009[Oxford Diffraction (2009). CrysAlis PRO. Oxford Diffraction Ltd, Yarnton, England.]) and Clark & Reid (1995[Clark, R. C. & Reid, J. S. (1995). Acta Cryst. A51, 887-897.])] Tmin = 0.990, Tmax = 0.994

  • 6900 measured reflections

  • 3025 independent reflections

  • 1509 reflections with I > 2σ(I)

  • Rint = 0.018
Refinement

  • R[F2 > 2σ(F2)] = 0.040

  • wR(F2) = 0.108

  • S = 0.83

  • 3025 reflections

  • 210 parameters

  • H-atom parameters constrained

  • Δρmax = 0.25 e Å−3

  • Δρmin = −0.13 e Å−3

Data collection: CrysAlis PRO (Oxford Diffraction, 2009[Oxford Diffraction (2009). CrysAlis PRO. Oxford Diffraction Ltd, Yarnton, England.]); cell refinement: CrysAlis PRO; data reduction: CrysAlis PRO; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); molecular graphics: SHELXTL (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); software used to prepare material for publication: publCIF (Westrip, 2010[Westrip, S. P. (2010). J. Appl. Cryst. 43. Submitted.]).

Supporting information

Crystal structure: contains datablocks I, global. DOI: https://doi.org/10.1107/S1600536810014728/hg2655sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536810014728/hg2655Isup2.hkl

checkCIF report


Comment top

β-keto esters are a class of potentially useful synthetic intermediates in the preparation of some physiologically active compounds. The medicinal values of this class of compounds have been demonstrated as antitumor, antianxiety, and antihypertension agents. General methods of β-keto ester preparation have been described in several publications including by March (1985), Shiosaki et al.(1981), and Matsumoto et al. (1973). Acyloin-type condensation reactions of α, β unsaturated esters have also been demonstrated in several publications of Totton et al. (1961), (1965), (1967), and Singh & Totton (1981). The mechanism of this condensation reaction was first suggested by Weidlich (1938) and confirmed by the successful synthesis of several adducts. Synthesis of the title compound was first performed by Totton et al. (1965). However, the compound has not previously been characterized by X-ray diffraction and therefore these studies were undertaken in order to elucidate details of the molecular structure. The title compound, C20H20O3, contains three chiral centers. These correspond to atom sites C2, C3, and C4 and contain R, S, and R configurations, respectively. The C—O bond lengths for the two carbonyl groups are 1.191 (2) and 1.198 (2) Å with the ring carbonyl having the slightly longer distance. The C—O bond in the ester group is quite a bit longer than the carbonyl distances, as expected, at 1.335 (2) Å. The aromatic C—C bond lengths in the phenyl groups are not extraordinary and average to 1.375 Å, while the C—C bonds in the cyclopentanone ring have an average distance of 1.525 Å indicative of the single bond nature. The molecular nature of the compound is preserved in the solid state. No significant interactions, e.g. H-bonding interactions, etc., are observed in the structure.

Related literature top

For the first synthesis of the title compound, see: Totton et al. (1965). For general methods of β-keto ester preparation, see: March (1985); Shiosaki et al.(1981); Matsumoto et al. (1973). For acyloin-type condensation reactions of α, β unsaturated esters, see: Totton et al. (1961, 1965, 1967); Singh & Totton (1981). The mechanism of this condensation reaction was first suggested by Weidlich (1938) and confirmed by the successful synthesis of several adducts.

Experimental top

The synthesis of the (1R,2S,3R)-ethyl 5-oxo-2,3-diphenylcyclopentanecarboxylate product was accomplished by modifi-cation of the prior procedure used by Totton (1961). Into a 1 L three necked round bottom flask fitted with a reflux condenser containing a CaCl2 drying tube was added 400 ml dry ether and 13 g of freshly prepared sodium sand, 50 g of ethyl cinnamate (287.1 mmol) was then added dropwise over a period of two hours. A series of color changes were observed where the initial light orange color changed to deep orange and finally to reddish brown. The mixture was stirred and refluxed overnight and cooled in an ice bath. While stirring, 70 ml of a 35% sulfuric acid was added carefully through an addition funnel. The reaction turned to yellow-orange color. The mixture was transferred to a large separatory funnel and the layers separated. The aqueous layer was then extracted with two – 75 ml portions of ether and combined to the original ether layer and which was then washed with four – 50 ml portions of a 20 % sodium carbonate solution and 100 ml water. The ether solution was dried over 50 g of anhydrous sodium sulfate, filtered by gravity, and the solvent removed with a rotatory evaporator. The sticky residue was dissolved in 200 ml of 95% ethanol and left for 1 hr at room temperature and kept in freezer overnight. The product was recrystallized several times from a 95% ethanol/water mixture. Yield was 10 %.

The compound is soluble in a number of organic solvents including diethyl ether, dichloromethane, methanol, ethanol etc, but found insoluble in hexane and hence single crystals for X-ray measurements were grown from an ether/hexane mixture.

The product was characterized using several spectroscopic techniques in addition to the X-ray analysis. The melting point was sharp (97-99 °C). 1H-NMR (DMSO): 7.2 m (10 H), 4.1 m (2 H), 3.9 t (1 H), 3.5 m (2 H), 2.98 q (1 H), 2.68 m (1 H), 1.2 m (3 H). IR spectrum: 2960-3057 cm-1 for C—H symmetric stretch; 1728, 1752 cm-1 for the C=O group and at ~1130 cm-1 for the C—O ether linkage. The 700-756 cm-1 region corresponds to the aromatic ring. The mass spectrum indicates a loss of the carbethoxy fragment from the molecular ion ( MW = 308), as represented by the peak with m/e of 236. Other stable fragment ions are represented by peaks at m/e of 178, 105, 104, and 77 indicating loss of various components of the material.

The compound shows a bright blue unstructured emission covering the 400-600 nm s pectral region at room temperature with the emission band maximizing at 460 nm. The excitation spectrum displays two broad bands at 310 nm and 405 nm. At liquid N2 temperature well defined bands are observed at 440 and 480 nm with a shoulder at 520 nm. The excitation band at liquid N2 temperature is also broad, centering at 380 nm. The overall emission spectrum is unaffected upon changing the excitation wavelength.

Refinement top

H-atoms were placed in calculated positions and allowed to ride during subsequent refinement, with Uiso(H) = 1.2Ueq(C) and C—H distances of 0.93 Å for the aromatic H atoms, with Uiso(H) = 1.2Ueq(C) and C—H distances of 0.98 Å for tertiary H atoms, with Uiso(H) = 1.2Ueq(C) and C—H distances of 0.97 Å for secondary H atoms, and with Uiso(H) = 1.5Ueq(C) and C—H distances of 0.96 Å for methyl H atoms. The terminal methyl group corresponding to C8 has a relatively large thermal ellipsoid corresponding to a high degree of thermal motion.

Structure description top

β-keto esters are a class of potentially useful synthetic intermediates in the preparation of some physiologically active compounds. The medicinal values of this class of compounds have been demonstrated as antitumor, antianxiety, and antihypertension agents. General methods of β-keto ester preparation have been described in several publications including by March (1985), Shiosaki et al.(1981), and Matsumoto et al. (1973). Acyloin-type condensation reactions of α, β unsaturated esters have also been demonstrated in several publications of Totton et al. (1961), (1965), (1967), and Singh & Totton (1981). The mechanism of this condensation reaction was first suggested by Weidlich (1938) and confirmed by the successful synthesis of several adducts. Synthesis of the title compound was first performed by Totton et al. (1965). However, the compound has not previously been characterized by X-ray diffraction and therefore these studies were undertaken in order to elucidate details of the molecular structure. The title compound, C20H20O3, contains three chiral centers. These correspond to atom sites C2, C3, and C4 and contain R, S, and R configurations, respectively. The C—O bond lengths for the two carbonyl groups are 1.191 (2) and 1.198 (2) Å with the ring carbonyl having the slightly longer distance. The C—O bond in the ester group is quite a bit longer than the carbonyl distances, as expected, at 1.335 (2) Å. The aromatic C—C bond lengths in the phenyl groups are not extraordinary and average to 1.375 Å, while the C—C bonds in the cyclopentanone ring have an average distance of 1.525 Å indicative of the single bond nature. The molecular nature of the compound is preserved in the solid state. No significant interactions, e.g. H-bonding interactions, etc., are observed in the structure.

For the first synthesis of the title compound, see: Totton et al. (1965). For general methods of β-keto ester preparation, see: March (1985); Shiosaki et al.(1981); Matsumoto et al. (1973). For acyloin-type condensation reactions of α, β unsaturated esters, see: Totton et al. (1961, 1965, 1967); Singh & Totton (1981). The mechanism of this condensation reaction was first suggested by Weidlich (1938) and confirmed by the successful synthesis of several adducts.

Computing details top

Data collection: CrysAlis PRO (Oxford Diffraction, 2009); cell refinement: CrysAlis PRO (Oxford Diffraction, 2009); data reduction: CrysAlis PRO (Oxford Diffraction, 2009); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: publCIF (Westrip, 2010).

Figures top
[Figure 1] Fig. 1. The molecular structure of I, with the atom-numbering scheme. Displacement ellipsoids for non-hydrogen atoms are drawn at the 50% probability level.
Ethyl 5-oxo-2,3-diphenylcyclopentane-1-carboxylate top
Crystal data top
C20H20O3F(000) = 1312
Mr = 308.36Dx = 1.191 Mg m−3
Monoclinic, C2/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -C 2ycCell parameters from 2093 reflections
a = 27.4961 (13) Åθ = 3.0–25.3°
b = 7.4008 (2) ŵ = 0.08 mm−1
c = 18.7063 (10) ÅT = 295 K
β = 115.389 (6)°Plate, colorless
V = 3439.0 (3) Å30.14 × 0.14 × 0.08 mm
Z = 8
Data collection top
Oxford Diffraction Xcalibur Eos
diffractometer		3025 independent reflections
Radiation source: fine-focus sealed tube1509 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.018
Detector resolution: 16.0514 pixels mm-1θmax = 25.0°, θmin = 3.0°
ω scansh = −32→31
Absorption correction: analytical
[CrysAlis PRO (Oxford Diffraction, 2009) and Clark & Reid (1995)]		k = −8→8
Tmin = 0.990, Tmax = 0.994l = −22→22
6900 measured reflections
Refinement top
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.040H-atom parameters constrained
wR(F2) = 0.108 w = 1/[σ2(Fo2) + (0.0618P)2]
where P = (Fo2 + 2Fc2)/3
S = 0.83(Δ/σ)max < 0.001
3025 reflectionsΔρmax = 0.25 e Å−3
210 parametersΔρmin = −0.13 e Å−3
0 restraintsExtinction correction: SHELXL97 (Sheldrick, 2008), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4
Primary atom site location: structure-invariant direct methodsExtinction coefficient: 0.0016 (4)
Crystal data top
C20H20O3V = 3439.0 (3) Å3
Mr = 308.36Z = 8
Monoclinic, C2/cMo Kα radiation
a = 27.4961 (13) ŵ = 0.08 mm−1
b = 7.4008 (2) ÅT = 295 K
c = 18.7063 (10) Å0.14 × 0.14 × 0.08 mm
β = 115.389 (6)°
Data collection top
Oxford Diffraction Xcalibur Eos
diffractometer		3025 independent reflections
Absorption correction: analytical
[CrysAlis PRO (Oxford Diffraction, 2009) and Clark & Reid (1995)]		1509 reflections with I > 2σ(I)
Tmin = 0.990, Tmax = 0.994Rint = 0.018
6900 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0400 restraints
wR(F2) = 0.108H-atom parameters constrained
S = 0.83Δρmax = 0.25 e Å−3
3025 reflectionsΔρmin = −0.13 e Å−3
210 parameters
Special details top

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > 2σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
C10.07043 (8)0.5517 (3)0.12865 (12)0.0674 (6)
C20.07109 (7)0.4093 (2)0.07003 (11)0.0555 (5)
H20.04590.44700.01670.067*
C30.12801 (6)0.4166 (2)0.07539 (10)0.0512 (5)
H30.15110.34190.12050.061*
C40.14455 (7)0.6168 (2)0.09701 (11)0.0556 (5)
H40.12600.68940.04910.067*
C50.12035 (7)0.6635 (2)0.15433 (12)0.0679 (6)
H5A0.14530.63420.20820.082*
H5B0.11170.79120.15150.082*
C60.05346 (8)0.2295 (3)0.08650 (12)0.0648 (6)
C7−0.02207 (10)0.0601 (3)0.0812 (2)0.1136 (10)
H7A−0.05510.02360.03690.136*
H7B0.0034−0.03890.09350.136*
C8−0.0323 (2)0.0926 (5)0.1442 (3)0.248 (3)
H8A0.00110.10170.19090.371*
H8B−0.0533−0.00470.15030.371*
H8C−0.05190.20380.13640.371*
C90.13429 (7)0.3507 (2)0.00345 (11)0.0555 (5)
C100.10049 (8)0.4082 (3)−0.07179 (12)0.0702 (6)
H100.07280.4883−0.07870.084*
C110.10716 (10)0.3488 (3)−0.13712 (14)0.0880 (7)
H110.08390.3884−0.18740.106*
C120.14780 (12)0.2323 (3)−0.12798 (17)0.0965 (8)
H120.15230.1922−0.17190.116*
C130.18164 (11)0.1751 (3)−0.05443 (18)0.0934 (7)
H130.20950.0963−0.04810.112*
C140.17513 (8)0.2328 (3)0.01133 (14)0.0759 (6)
H140.19850.19160.06130.091*
C150.20420 (7)0.6534 (2)0.12792 (11)0.0533 (5)
C160.22364 (8)0.7672 (3)0.08826 (13)0.0715 (6)
H160.19980.82020.04120.086*
C170.27797 (10)0.8043 (3)0.11702 (16)0.0886 (7)
H170.29040.88240.08950.106*
C180.31355 (9)0.7261 (3)0.18599 (16)0.0832 (7)
H180.35020.75070.20550.100*
C190.29501 (8)0.6119 (3)0.22596 (13)0.0757 (6)
H190.31910.55790.27260.091*
C200.24114 (8)0.5764 (2)0.19776 (12)0.0655 (6)
H200.22900.49930.22590.079*
O10.03553 (6)0.5692 (2)0.15029 (11)0.1100 (6)
O20.08328 (6)0.10985 (18)0.12097 (10)0.1022 (6)
O3−0.00002 (5)0.21897 (16)0.05868 (9)0.0815 (5)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
C10.0573 (13)0.0655 (12)0.0769 (15)0.0007 (11)0.0264 (11)−0.0052 (11)
C20.0520 (11)0.0482 (10)0.0563 (11)−0.0013 (9)0.0139 (9)0.0025 (9)
C30.0451 (10)0.0444 (10)0.0538 (11)0.0029 (8)0.0114 (8)0.0026 (8)
C40.0514 (11)0.0451 (10)0.0611 (12)0.0034 (9)0.0154 (9)0.0030 (9)
C50.0612 (12)0.0552 (11)0.0809 (15)−0.0014 (10)0.0243 (11)−0.0128 (10)
C60.0547 (13)0.0601 (13)0.0678 (14)−0.0045 (11)0.0150 (10)0.0008 (11)
C70.112 (2)0.0680 (14)0.178 (3)−0.0309 (14)0.078 (2)−0.0002 (17)
C80.460 (8)0.151 (3)0.270 (6)−0.108 (4)0.289 (6)−0.023 (3)
C90.0551 (11)0.0477 (10)0.0594 (13)−0.0071 (9)0.0205 (10)−0.0030 (9)
C100.0690 (13)0.0769 (13)0.0612 (14)0.0009 (11)0.0244 (11)0.0017 (11)
C110.1040 (18)0.0914 (16)0.0651 (16)−0.0094 (15)0.0329 (13)0.0038 (13)
C120.136 (2)0.0823 (16)0.094 (2)−0.0037 (17)0.0707 (19)−0.0059 (15)
C130.1072 (19)0.0830 (15)0.106 (2)0.0188 (14)0.0606 (17)−0.0007 (16)
C140.0782 (14)0.0709 (13)0.0797 (16)0.0135 (12)0.0350 (12)−0.0014 (12)
C150.0521 (11)0.0426 (10)0.0593 (12)−0.0023 (9)0.0182 (10)−0.0046 (9)
C160.0681 (14)0.0692 (12)0.0725 (15)−0.0103 (11)0.0256 (11)0.0051 (11)
C170.0874 (18)0.0887 (16)0.100 (2)−0.0273 (14)0.0499 (15)−0.0109 (15)
C180.0583 (14)0.0838 (15)0.104 (2)−0.0127 (12)0.0314 (15)−0.0300 (15)
C190.0606 (14)0.0659 (12)0.0816 (15)0.0022 (11)0.0124 (12)−0.0103 (12)
C200.0557 (12)0.0570 (11)0.0691 (14)−0.0032 (10)0.0126 (10)0.0010 (10)
O10.0867 (12)0.1232 (13)0.1423 (16)−0.0258 (10)0.0702 (11)−0.0533 (11)
O20.0727 (10)0.0656 (9)0.1337 (15)−0.0009 (8)0.0113 (9)0.0322 (9)
O30.0626 (9)0.0668 (8)0.1157 (13)−0.0089 (7)0.0388 (8)0.0037 (8)
Geometric parameters (Å, º) top
C1—O11.198 (2)C9—C141.379 (2)
C1—C51.495 (2)C9—C101.380 (3)
C1—C21.527 (3)C10—C111.383 (3)
C2—C61.493 (2)C10—H100.9300
C2—C31.526 (2)C11—C121.363 (3)
C2—H20.9800C11—H110.9300
C3—C91.509 (2)C12—C131.356 (3)
C3—C41.552 (2)C12—H120.9300
C3—H30.9800C13—C141.384 (3)
C4—C151.511 (2)C13—H130.9300
C4—C51.525 (3)C14—H140.9300
C4—H40.9800C15—C161.373 (3)
C5—H5A0.9700C15—C201.388 (2)
C5—H5B0.9700C16—C171.381 (3)
C6—O21.191 (2)C16—H160.9300
C6—O31.335 (2)C17—C181.369 (3)
C7—C81.344 (4)C17—H170.9300
C7—O31.465 (2)C18—C191.364 (3)
C7—H7A0.9700C18—H180.9300
C7—H7B0.9700C19—C201.368 (3)
C8—H8A0.9600C19—H190.9300
C8—H8B0.9600C20—H200.9300
C8—H8C0.9600
O1—C1—C5126.14 (19)H8A—C8—H8C109.5
O1—C1—C2125.13 (18)H8B—C8—H8C109.5
C5—C1—C2108.73 (17)C14—C9—C10117.8 (2)
C6—C2—C3115.64 (15)C14—C9—C3120.56 (17)
C6—C2—C1111.23 (16)C10—C9—C3121.67 (17)
C3—C2—C1104.83 (14)C9—C10—C11121.1 (2)
C6—C2—H2108.3C9—C10—H10119.5
C3—C2—H2108.3C11—C10—H10119.5
C1—C2—H2108.3C12—C11—C10120.2 (2)
C9—C3—C2115.86 (14)C12—C11—H11119.9
C9—C3—C4114.09 (15)C10—C11—H11119.9
C2—C3—C4103.23 (13)C13—C12—C11119.6 (2)
C9—C3—H3107.7C13—C12—H12120.2
C2—C3—H3107.7C11—C12—H12120.2
C4—C3—H3107.7C12—C13—C14120.8 (2)
C15—C4—C5114.81 (15)C12—C13—H13119.6
C15—C4—C3114.83 (13)C14—C13—H13119.6
C5—C4—C3103.44 (14)C9—C14—C13120.6 (2)
C15—C4—H4107.8C9—C14—H14119.7
C5—C4—H4107.8C13—C14—H14119.7
C3—C4—H4107.8C16—C15—C20117.59 (17)
C1—C5—C4105.42 (16)C16—C15—C4120.89 (16)
C1—C5—H5A110.7C20—C15—C4121.51 (17)
C4—C5—H5A110.7C15—C16—C17121.2 (2)
C1—C5—H5B110.7C15—C16—H16119.4
C4—C5—H5B110.7C17—C16—H16119.4
H5A—C5—H5B108.8C18—C17—C16120.0 (2)
O2—C6—O3123.72 (18)C18—C17—H17120.0
O2—C6—C2124.42 (17)C16—C17—H17120.0
O3—C6—C2111.86 (17)C19—C18—C17119.6 (2)
C8—C7—O3112.1 (2)C19—C18—H18120.2
C8—C7—H7A109.2C17—C18—H18120.2
O3—C7—H7A109.2C18—C19—C20120.3 (2)
C8—C7—H7B109.2C18—C19—H19119.8
O3—C7—H7B109.2C20—C19—H19119.8
H7A—C7—H7B107.9C19—C20—C15121.2 (2)
C7—C8—H8A109.5C19—C20—H20119.4
C7—C8—H8B109.5C15—C20—H20119.4
H8A—C8—H8B109.5C6—O3—C7117.20 (17)
C7—C8—H8C109.5

Experimental details

Crystal data
Chemical formulaC20H20O3
Mr308.36
Crystal system, space groupMonoclinic, C2/c
Temperature (K)295
a, b, c (Å)27.4961 (13), 7.4008 (2), 18.7063 (10)
β (°) 115.389 (6)
V (Å3)3439.0 (3)
Z8
Radiation typeMo Kα
µ (mm−1)0.08
Crystal size (mm)0.14 × 0.14 × 0.08
Data collection
DiffractometerOxford Diffraction Xcalibur Eos
Absorption correctionAnalytical
[CrysAlis PRO (Oxford Diffraction, 2009) and Clark & Reid (1995)]
Tmin, Tmax0.990, 0.994
No. of measured, independent and
observed [I > 2σ(I)] reflections		6900, 3025, 1509
Rint0.018
(sin θ/λ)max (Å−1)0.595
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.040, 0.108, 0.83
No. of reflections3025
No. of parameters210
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å−3)0.25, −0.13

Computer programs: CrysAlis PRO (Oxford Diffraction, 2009), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008), publCIF (Westrip, 2010).

 

Acknowledgements

Support by the NOAA–EPP award number NA06OAR4810187 to NCAT and by the ACS–PRF is gratefully acknowledged by ZA. The authors also acknowledge the National Science Foundation for their generous support (NSF-CAREER grant to RES, CHE-0846680).

References

First citationClark, R. C. & Reid, J. S. (1995). Acta Cryst. A51, 887–897.  CrossRef CAS Web of Science IUCr Journals Google Scholar
 First citationMarch, J. (1985). Advanced Organic Chemistry, 3rd ed. New York: John Wiley and Sons.  Google Scholar
 First citationMatsumoto, K., Suzuki, M., Iwasaki, T. & Miyoshi, M. (1973). J. Org. Chem. 38, 2731.  CrossRef Web of Science Google Scholar
 First citationOxford Diffraction (2009). CrysAlis PRO. Oxford Diffraction Ltd, Yarnton, England.  Google Scholar
 First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationShiosaki, K., Fels, G. & Rapoport, H. (1981). J. Org. Chem. 46, 3230–3234.  CrossRef CAS Web of Science Google Scholar
 First citationSingh, P. & Totton, E. L. (1981). Cryst. Struct. Commun. 10, 739–743.  CAS Google Scholar
 First citationTotton, E. L., Camp, N. C., Cooper, G. M., Haywood, B. D. & Lewis, D. P. (1967). J. Org. Chem. 32, 2033–2034.  Google Scholar
 First citationTotton, E. L., Freeman, R. C., Powell, H. & Yarboro, T. L. (1961). J. Org. Chem. 26, 343–346.  CrossRef CAS Web of Science Google Scholar
 First citationTotton, E. L., Kilpatri, G. R., Horton, N. & Blakeney, S. A. (1965). J. Org. Chem. 30, 1647–1648.  CrossRef CAS Web of Science Google Scholar
 First citationWeidlich, H. A. (1938). Berichte, 71, 1601–1603.  Google Scholar
 First citationWestrip, S. P. (2010). J. Appl. Cryst. 43. Submitted.  Google Scholar

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ISSN: 2056-9890
Volume 66| Part 5| May 2010| Page o1183
https://doi.org/10.1107/S1600536810014728
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