7,7-Dimethyl-4a-(3-methyl-2-buten­yl)-2-oxo-4a,5,6,7-tetra­hydro-2H-chromen-4-yl benzoate

Möws, K.; Schürmann, M.; Preut, H.; Plietker, B.

doi:10.1107/S1600536809030918

organic compounds

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ISSN: 2056-9890

Volume 65| Part 9| September 2009| Page o2139

doi:10.1107/S1600536809030918

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7,7-Dimethyl-4a-(3-methyl-2-butenyl)-2-oxo-4a,5,6,7-tetrahydro-2H-chromen-4-yl benzoate

Katrin Möws,^a,^b Markus Schürmann,^a Hans Preut ^a ^* and Bernd Plietker ^a,^b

^aFakultät Chemie, Technische Universität Dortmund, Otto-Hahn-Strasse 6, 44221 Dortmund, Germany, and ^bInstitut für Organische Chemie, Fakultät Chemie, Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany
^*Correspondence e-mail: hans.preut@udo.edu

(Received 28 July 2009; accepted 4 August 2009; online 12 August 2009)

An intramolecular Claisen-like cyclization of ethyl 2-acetoxy-4,4-dimethyl-1-(3-methylbut-2-enyl)cyclohex-2-enecarboxylate followed by dialkylation yielded the bicyclic title compound, C₂₃H₂₆O₄. In both of the fused six-membered rings exist fragments of four atoms which are planar, whereas the remaining two atoms deviate by up to 0.682 (3) Å on one side of the plane of the ring containing an O atom and by up to 0.415 (3) Å on opposite sides of the other ring. The dihedral anglebetween the planar fragments of the six-membered rings is 41.76 (10)°

Related literature

For literature related to the synthesis, see: Ciochina & Grossman (2006 ).

Experimental

Crystal data

C₂₃H₂₆O₄
M_r = 366.44
Triclinic, $[P \overline 1]$
a = 9.559 (4) Å
b = 10.201 (5) Å
c = 11.087 (5) Å
α = 69.23 (2)°
β = 83.649 (17)°
γ = 74.823 (17)°
V = 975.4 (8) Å³
Z = 2
Mo Kα radiation
μ = 0.08 mm⁻¹
T = 173 K
0.45 × 0.40 × 0.20 mm

Data collection

Nonius KappaCCD diffractometer
Absorption correction: none
12665 measured reflections
3547 independent reflections
1691 reflections with I > 2σ(I)
R_int = 0.065

Refinement

R[F² > 2σ(F²)] = 0.043
wR(F²) = 0.067
S = 0.81
3547 reflections
248 parameters
H-atom parameters constrained
Δρ_max = 0.17 e Å⁻³
Δρ_min = −0.14 e Å⁻³

Data collection: COLLECT (Nonius, 1998 ); cell refinement: DENZO and SCALEPACK (Otwinowski & Minor, 1997 ); data reduction: DENZO and SCALEPACK; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL-Plus (Sheldrick, 2008); software used to prepare material for publication: SHELXL97 and PLATON (Spek, 2009 ).

Supporting information

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536809030918/hg2544sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536809030918/hg2544Isup2.hkl

checkCIF report

Related literature top

For literature related to the synthesis, see: Ciochina & Grossman (2006).

Experimental top

Diethylether was dryed over sodium. All other solvents and reagents were commercially available and used as received. Flash-chromatography was done on silicagel 60 (230–400 mesh) using head pressure by means of compressed air. Infrared spectra (IR) were recorded as a thin film between KBr-plates. The instrument used was a Bruker IFS 66 F T—IR spectrophotometer. GC—MS spectra were recorded on a Finnigan Polaris GCQ spectrometer. Proton (¹H NMR, 500 MHz) and carbon (¹³C NMR, 125 MHz) nuclear magnetic resonance spectra were recorded in chloroform(d-1) and referenced to the solvent signal. The instrument used was a Bruker DRX 500. The multiplicities of the signals are given as s (singlet), d (doublet), t (triplet), and m (multiplet).

HMDS (468 µL, 2.25 mmol) was dissolved in diethylether (3 ml) at 273 K. Butyllithium (1.3 ml, 2.03 mmol, 1.6 M in hexane) was added at that temperature and the mixture was stirred for 15 minutes. After cooling to 195 K a suspension of CuI (216 mg, 1.13 mmol) and ethyl 2-acetoxy-4,4-dimethyl-1-(3-methylbut-2-enyl)cyclohex-2-enecarboxylate (348 mg, 1.13 mmol) in diethylether (3 ml) was added. The mixture was stirred for 2 h. Benzoyl chloride (88 µl, 2.25 mmol) was added dropwise and the mixture was stirred for 5 days at room temperature. An aqueous Seignette salt-solution was added. Phase were separated and the aqueous layer was extracted with Et₂O (3 x 10 ml). The combined organic layers were dried over Na₂SO₄ and concentrated in vacuum (Ciochina & Grossman, 2006). The crude product was purified via column chromatography (10:1 i-hexane/ethyl acetate). The product was obtained in 12% yield (50 mg, 0.136 mmol). The purified product was crystallized by slow evaporation of a mixture of diethylether and i-hexane.

R_f: 0.22 (i-hexane/ethyl acetate 10:1), mp: 387 K, ¹H NMR (400 MHz, CDCl₃): δ (p.p.m.) = 8.08–7.50 (m, 5H, CH), 6.33 (s, 1H, CH), 5.28 (s, 1H, CH), 5.21 (m, 1H, CH), 2.62 (dd, J = 13.9, 7.7 Hz, 1H, CH₂), 2.43 (dd, J = 13.9, 8.5 Hz, 1H, CH₂), 2.06 (dt, J = 13.4, 3.5 Hz, 1H, CH₂), 1.72 (dt, J = 13.9, 3.0 Hz, 1H, CH₂), 1.65 (s, 3H, CH₃), 1.59 (s, 3H, CH₃), 1.57–1.52 (m, 1H, CH₂), 1.10 (s, 3H, CH₃), 1.03 (s, 3H, CH₃). ¹³C NMR (125 MHz, CDCl₃): δ (p.p.m.) = 168.7, 162.9, 162.4, 147.8, 136.8, 134.5, 130.4, 129.0, 120.3, 118.3, 105.1, 42.3, 36.7, 32.8, 31.9, 31.2, 26.5, 26.1. IR (film): ν (cm^-1) = 2966 (m), 2945 (m), 2919 (m), 2863 (m), 1759 (s), 1736 (s), 1673 (m), 1636 (m), 1452 (m), 1366 (m), 1234 (s), 1145 (s), 1077 (s), 1065 (s), 1020 (m). MS (EI, 70 eV): m / z (%) = 366 (10) [M+], 351 (1) [C₂₂H₂₃O₄⁺], 311 (1) [C₁₉H₁₉O₄⁺], 261 (100) [C₁₆H₂₁O₃⁺], 245 (5) [C₁₆H₂₁O₂⁺], 219 (2) [C₁₃H₁₅O₃⁺], 121 (1) [C₇H₅O₂⁺], 105 (99) [C₇H₅O⁺], 77 (26) [C₆H₅⁺]. LRMS (FAB⁺LR,C₂₃H₂₆O₄) calc. [(M+H)⁺]: 367.18; found: 367.02.

Computing details top

Data collection: COLLECT (Nonius, 1998); cell refinement: DENZO and SCALEPACK (Otwinowski & Minor, 1997); data reduction: DENZO and SCALEPACK (Otwinowski & Minor, 1997); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL-Plus (Sheldrick, 2008); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008) and PLATON (Spek, 2009).

Figures top

Fig. 1. : The asymmetric unit of the title compound showing the labelling of all non-H atoms. Displacement ellipsoids are shown at the 30% probability level. Of the two disordered positions C35 and C35' only one is shown.

7,7-Dimethyl-4a-(3-methyl-2-butenyl)-2-oxo-4a,5,6,7-tetrahydro-2H- chromen-4-yl benzoate top

Crystal data top

C₂₃H₂₆O₄	Z = 2
M_r = 366.44	F(000) = 392
Triclinic, P1	D_x = 1.248 Mg m⁻³
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71073 Å
a = 9.559 (4) Å	Cell parameters from 12656 reflections
b = 10.201 (5) Å	θ = 2.9–25.3°
c = 11.087 (5) Å	µ = 0.08 mm⁻¹
α = 69.23 (2)°	T = 173 K
β = 83.649 (17)°	Block, colourless
γ = 74.823 (17)°	0.45 × 0.40 × 0.20 mm
V = 975.4 (8) Å³

Data collection top

Nonius KappaCCD diffractometer	1691 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tube	R_int = 0.065
Graphite monochromator	θ_max = 25.3°, θ_min = 2.9°
Detector resolution: 19 vertical, 18 horizontal pixels mm^-1	h = −11→11
239 frames via ω–rotation (Δω=2°) and two times 20 s per frame (four sets at different κ–angles) scans	k = −11→12
12665 measured reflections	l = −13→13
3547 independent reflections

Refinement top

Refinement on F²	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F² > 2σ(F²)] = 0.043	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.067	H-atom parameters constrained
S = 0.81	w = 1/[σ²(F_o²)]
3547 reflections	(Δ/σ)_max < 0.001
248 parameters	Δρ_max = 0.17 e Å⁻³
0 restraints	Δρ_min = −0.14 e Å⁻³

Crystal data top

C₂₃H₂₆O₄	γ = 74.823 (17)°
M_r = 366.44	V = 975.4 (8) Å³
Triclinic, P1	Z = 2
a = 9.559 (4) Å	Mo Kα radiation
b = 10.201 (5) Å	µ = 0.08 mm⁻¹
c = 11.087 (5) Å	T = 173 K
α = 69.23 (2)°	0.45 × 0.40 × 0.20 mm
β = 83.649 (17)°

Data collection top

Nonius KappaCCD diffractometer	1691 reflections with I > 2σ(I)
12665 measured reflections	R_int = 0.065
3547 independent reflections

Refinement top

R[F² > 2σ(F²)] = 0.043	0 restraints
wR(F²) = 0.067	H-atom parameters constrained
S = 0.81	Δρ_max = 0.17 e Å⁻³
3547 reflections	Δρ_min = −0.14 e Å⁻³
248 parameters

Special details top

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

	x	y	z	U_iso*/U_eq
O1	0.57097 (14)	0.80118 (14)	−0.03317 (12)	0.0520 (4)
O2	0.46540 (13)	0.63064 (14)	0.09192 (11)	0.0425 (4)
O3	0.14946 (14)	0.93092 (13)	0.21014 (11)	0.0436 (4)
O4	0.08624 (14)	1.10136 (14)	0.01484 (13)	0.0592 (4)
C1	0.2779 (2)	0.6848 (2)	0.25269 (17)	0.0372 (5)
C2	0.2597 (2)	0.8390 (2)	0.16647 (17)	0.0386 (5)
C3	0.3498 (2)	0.8812 (2)	0.06716 (17)	0.0420 (5)
H3A	0.3364	0.9805	0.0163	0.050*
C4	0.4696 (2)	0.7729 (2)	0.03743 (18)	0.0424 (6)
C5	0.3483 (2)	0.5906 (2)	0.17409 (17)	0.0374 (5)
C6	0.3123 (2)	0.4741 (2)	0.17565 (16)	0.0403 (5)
H6A	0.3664	0.4240	0.1214	0.048*
C7	0.1911 (2)	0.4141 (2)	0.25740 (17)	0.0427 (5)
C8	0.1416 (2)	0.48837 (19)	0.35812 (17)	0.0438 (5)
H8A	0.0457	0.4717	0.3940	0.053*
H8B	0.2110	0.4442	0.4297	0.053*
C9	0.1305 (2)	0.65023 (19)	0.30311 (17)	0.0423 (5)
H9A	0.0926	0.6932	0.3710	0.051*
H9B	0.0608	0.6948	0.2317	0.051*
C10	0.0654 (2)	0.4414 (2)	0.16994 (17)	0.0564 (6)
H10A	0.1009	0.4002	0.1016	0.085*
H10B	0.0254	0.5456	0.1311	0.085*
H10C	−0.0104	0.3960	0.2212	0.085*
C11	0.2449 (2)	0.25092 (19)	0.32494 (17)	0.0554 (6)
H11A	0.2777	0.2040	0.2601	0.083*
H11B	0.1657	0.2123	0.3771	0.083*
H11C	0.3256	0.2321	0.3808	0.083*
C12	0.3724 (2)	0.6598 (2)	0.36940 (16)	0.0435 (5)
H12A	0.3274	0.7340	0.4095	0.052*
H12B	0.3699	0.5644	0.4347	0.052*
C13	0.5899 (2)	0.7717 (2)	0.32049 (17)	0.0432 (5)
C14	0.5284 (2)	0.6650 (2)	0.33670 (16)	0.0437 (5)
H14A	0.5908	0.5802	0.3264	0.052*
C15	0.7482 (2)	0.7596 (2)	0.28583 (18)	0.0613 (7)
H15A	0.7934	0.6623	0.2839	0.092*
H15B	0.7957	0.7777	0.3503	0.092*
H15C	0.7589	0.8308	0.2007	0.092*
C16	0.5118 (2)	0.9153 (2)	0.33373 (17)	0.0561 (6)
H16A	0.4091	0.9170	0.3540	0.084*
H16B	0.5209	0.9931	0.2525	0.084*
H16C	0.5548	0.9291	0.4033	0.084*
C21	−0.0634 (2)	1.1136 (2)	0.19952 (18)	0.0364 (5)
C22	−0.0832 (2)	1.0524 (2)	0.33214 (17)	0.0460 (6)
H22A	−0.0149	0.9691	0.3809	0.055*
C23	−0.2037 (2)	1.1143 (2)	0.39196 (19)	0.0520 (6)
H23A	−0.2180	1.0729	0.4824	0.062*
C24	−0.3031 (2)	1.2347 (2)	0.3223 (2)	0.0518 (6)
H24A	−0.3854	1.2758	0.3649	0.062*
C25	−0.2839 (2)	1.2966 (2)	0.19050 (19)	0.0496 (6)
H25A	−0.3526	1.3798	0.1421	0.059*
C26	−0.1632 (2)	1.2356 (2)	0.13033 (18)	0.0445 (5)
H26A	−0.1487	1.2781	0.0400	0.053*
C27	0.0632 (2)	1.0537 (2)	0.1279 (2)	0.0422 (5)

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
O1	0.0492 (10)	0.0545 (10)	0.0489 (9)	−0.0150 (8)	0.0184 (8)	−0.0175 (8)
O2	0.0430 (9)	0.0443 (9)	0.0372 (8)	−0.0111 (8)	0.0074 (7)	−0.0122 (7)
O3	0.0457 (9)	0.0418 (9)	0.0353 (8)	0.0002 (7)	0.0020 (7)	−0.0118 (7)
O4	0.0581 (11)	0.0648 (11)	0.0345 (9)	−0.0001 (8)	0.0044 (8)	−0.0049 (8)
C1	0.0352 (13)	0.0413 (13)	0.0327 (12)	−0.0075 (11)	0.0046 (10)	−0.0124 (10)
C2	0.0388 (14)	0.0386 (14)	0.0359 (12)	−0.0029 (11)	−0.0013 (11)	−0.0141 (11)
C3	0.0446 (14)	0.0410 (13)	0.0367 (12)	−0.0068 (11)	0.0022 (11)	−0.0120 (10)
C4	0.0491 (16)	0.0439 (15)	0.0321 (13)	−0.0131 (13)	0.0013 (11)	−0.0097 (11)
C5	0.0363 (14)	0.0414 (14)	0.0293 (12)	−0.0099 (11)	0.0023 (10)	−0.0062 (10)
C6	0.0432 (14)	0.0431 (14)	0.0326 (12)	−0.0082 (12)	0.0032 (10)	−0.0131 (10)
C7	0.0450 (14)	0.0433 (14)	0.0379 (12)	−0.0109 (12)	0.0019 (11)	−0.0124 (11)
C8	0.0441 (14)	0.0475 (14)	0.0387 (12)	−0.0137 (11)	0.0062 (10)	−0.0133 (11)
C9	0.0411 (14)	0.0486 (14)	0.0352 (12)	−0.0078 (11)	0.0043 (10)	−0.0154 (10)
C10	0.0586 (16)	0.0652 (16)	0.0495 (14)	−0.0228 (13)	0.0018 (13)	−0.0197 (12)
C11	0.0642 (16)	0.0468 (14)	0.0504 (14)	−0.0153 (13)	0.0086 (12)	−0.0122 (11)
C12	0.0496 (15)	0.0458 (14)	0.0330 (12)	−0.0120 (12)	0.0012 (11)	−0.0110 (10)
C13	0.0446 (15)	0.0510 (15)	0.0308 (12)	−0.0122 (13)	−0.0014 (10)	−0.0092 (11)
C14	0.0449 (15)	0.0474 (14)	0.0327 (12)	−0.0048 (12)	−0.0036 (11)	−0.0099 (11)
C15	0.0491 (16)	0.0791 (18)	0.0491 (14)	−0.0152 (13)	−0.0003 (12)	−0.0141 (12)
C16	0.0627 (16)	0.0566 (15)	0.0473 (13)	−0.0165 (13)	0.0000 (12)	−0.0143 (11)
C21	0.0355 (13)	0.0374 (13)	0.0352 (12)	−0.0069 (11)	0.0019 (10)	−0.0133 (10)
C22	0.0450 (15)	0.0465 (14)	0.0385 (13)	−0.0026 (12)	−0.0001 (11)	−0.0110 (11)
C23	0.0543 (16)	0.0579 (16)	0.0393 (13)	−0.0048 (13)	0.0042 (12)	−0.0188 (12)
C24	0.0419 (15)	0.0588 (16)	0.0540 (15)	−0.0029 (13)	0.0039 (12)	−0.0264 (13)
C25	0.0428 (15)	0.0520 (15)	0.0480 (15)	−0.0006 (12)	−0.0073 (12)	−0.0158 (12)
C26	0.0432 (14)	0.0456 (14)	0.0400 (12)	−0.0055 (12)	−0.0041 (11)	−0.0115 (11)
C27	0.0396 (14)	0.0412 (14)	0.0410 (13)	−0.0042 (11)	−0.0052 (12)	−0.0110 (12)

Geometric parameters (Å, º) top

O1—C4	1.206 (2)	C11—H11B	0.9800
O2—C4	1.369 (2)	C11—H11C	0.9800
O2—C5	1.414 (2)	C12—C14	1.505 (2)
O3—C27	1.377 (2)	C12—H12A	0.9900
O3—C2	1.3843 (19)	C12—H12B	0.9900
O4—C27	1.191 (2)	C13—C14	1.317 (2)
C1—C2	1.498 (2)	C13—C15	1.504 (2)
C1—C5	1.504 (2)	C13—C16	1.510 (2)
C1—C9	1.539 (2)	C14—H14A	0.9500
C1—C12	1.568 (2)	C15—H15A	0.9800
C2—C3	1.337 (2)	C15—H15B	0.9800
C3—C4	1.468 (2)	C15—H15C	0.9800
C3—H3A	0.9500	C16—H16A	0.9800
C5—C6	1.316 (2)	C16—H16B	0.9800
C6—C7	1.511 (2)	C16—H16C	0.9800
C6—H6A	0.9500	C21—C26	1.382 (2)
C7—C8	1.530 (2)	C21—C22	1.392 (2)
C7—C11	1.532 (2)	C21—C27	1.487 (2)
C7—C10	1.534 (2)	C22—C23	1.383 (2)
C8—C9	1.522 (2)	C22—H22A	0.9500
C8—H8A	0.9900	C23—C24	1.373 (2)
C8—H8B	0.9900	C23—H23A	0.9500
C9—H9A	0.9900	C24—C25	1.384 (2)
C9—H9B	0.9900	C24—H24A	0.9500
C10—H10A	0.9800	C25—C26	1.383 (2)
C10—H10B	0.9800	C25—H25A	0.9500
C10—H10C	0.9800	C26—H26A	0.9500
C11—H11A	0.9800

C4—O2—C5	120.47 (15)	H11A—C11—H11B	109.5
C27—O3—C2	122.64 (14)	C7—C11—H11C	109.5
C2—C1—C5	107.80 (15)	H11A—C11—H11C	109.5
C2—C1—C9	111.32 (16)	H11B—C11—H11C	109.5
C5—C1—C9	107.82 (16)	C14—C12—C1	115.38 (15)
C2—C1—C12	107.95 (16)	C14—C12—H12A	108.4
C5—C1—C12	112.42 (15)	C1—C12—H12A	108.4
C9—C1—C12	109.54 (14)	C14—C12—H12B	108.4
C3—C2—O3	125.00 (17)	C1—C12—H12B	108.4
C3—C2—C1	122.81 (17)	H12A—C12—H12B	107.5
O3—C2—C1	111.89 (16)	C14—C13—C15	121.7 (2)
C2—C3—C4	119.40 (18)	C14—C13—C16	124.62 (19)
C2—C3—H3A	120.3	C15—C13—C16	113.69 (19)
C4—C3—H3A	120.3	C13—C14—C12	128.56 (19)
O1—C4—O2	117.76 (19)	C13—C14—H14A	115.7
O1—C4—C3	124.16 (19)	C12—C14—H14A	115.7
O2—C4—C3	118.08 (18)	C13—C15—H15A	109.5
C6—C5—O2	117.13 (17)	C13—C15—H15B	109.5
C6—C5—C1	126.20 (18)	H15A—C15—H15B	109.5
O2—C5—C1	116.66 (17)	C13—C15—H15C	109.5
C5—C6—C7	124.84 (18)	H15A—C15—H15C	109.5
C5—C6—H6A	117.6	H15B—C15—H15C	109.5
C7—C6—H6A	117.6	C13—C16—H16A	109.5
C6—C7—C8	109.01 (16)	C13—C16—H16B	109.5
C6—C7—C11	109.75 (16)	H16A—C16—H16B	109.5
C8—C7—C11	109.79 (16)	C13—C16—H16C	109.5
C6—C7—C10	108.99 (15)	H16A—C16—H16C	109.5
C8—C7—C10	110.54 (16)	H16B—C16—H16C	109.5
C11—C7—C10	108.74 (17)	C26—C21—C22	119.58 (18)
C9—C8—C7	112.82 (15)	C26—C21—C27	117.90 (17)
C9—C8—H8A	109.0	C22—C21—C27	122.51 (18)
C7—C8—H8A	109.0	C23—C22—C21	119.15 (19)
C9—C8—H8B	109.0	C23—C22—H22A	120.4
C7—C8—H8B	109.0	C21—C22—H22A	120.4
H8A—C8—H8B	107.8	C24—C23—C22	120.90 (19)
C8—C9—C1	112.10 (15)	C24—C23—H23A	119.6
C8—C9—H9A	109.2	C22—C23—H23A	119.6
C1—C9—H9A	109.2	C23—C24—C25	120.33 (19)
C8—C9—H9B	109.2	C23—C24—H24A	119.8
C1—C9—H9B	109.2	C25—C24—H24A	119.8
H9A—C9—H9B	107.9	C26—C25—C24	119.00 (19)
C7—C10—H10A	109.5	C26—C25—H25A	120.5
C7—C10—H10B	109.5	C24—C25—H25A	120.5
H10A—C10—H10B	109.5	C21—C26—C25	121.03 (18)
C7—C10—H10C	109.5	C21—C26—H26A	119.5
H10A—C10—H10C	109.5	C25—C26—H26A	119.5
H10B—C10—H10C	109.5	O4—C27—O3	123.95 (18)
C7—C11—H11A	109.5	O4—C27—C21	125.59 (19)
C7—C11—H11B	109.5	O3—C27—C21	110.43 (17)

C27—O3—C2—C3	39.7 (3)	C6—C7—C8—C9	42.2 (2)
C27—O3—C2—C1	−146.56 (16)	C11—C7—C8—C9	162.48 (16)
C5—C1—C2—C3	−29.9 (3)	C10—C7—C8—C9	−77.6 (2)
C9—C1—C2—C3	−147.98 (18)	C7—C8—C9—C1	−62.2 (2)
C12—C1—C2—C3	91.8 (2)	C2—C1—C9—C8	163.77 (15)
C5—C1—C2—O3	156.15 (15)	C5—C1—C9—C8	45.7 (2)
C9—C1—C2—O3	38.1 (2)	C12—C1—C9—C8	−76.91 (19)
C12—C1—C2—O3	−82.17 (19)	C2—C1—C12—C14	−68.5 (2)
O3—C2—C3—C4	175.08 (16)	C5—C1—C12—C14	50.2 (2)
C1—C2—C3—C4	2.0 (3)	C9—C1—C12—C14	170.09 (16)
C5—O2—C4—O1	−179.08 (16)	C15—C13—C14—C12	−179.07 (16)
C5—O2—C4—C3	0.1 (2)	C16—C13—C14—C12	0.7 (3)
C2—C3—C4—O1	−165.68 (19)	C1—C12—C14—C13	100.6 (2)
C2—C3—C4—O2	15.2 (3)	C26—C21—C22—C23	0.6 (3)
C4—O2—C5—C6	149.39 (17)	C27—C21—C22—C23	180.00 (18)
C4—O2—C5—C1	−31.3 (2)	C21—C22—C23—C24	−0.1 (3)
C2—C1—C5—C6	−137.1 (2)	C22—C23—C24—C25	−0.2 (3)
C9—C1—C5—C6	−16.8 (3)	C23—C24—C25—C26	−0.1 (3)
C12—C1—C5—C6	104.0 (2)	C22—C21—C26—C25	−1.0 (3)
C2—C1—C5—O2	43.7 (2)	C27—C21—C26—C25	179.64 (17)
C9—C1—C5—O2	163.97 (14)	C24—C25—C26—C21	0.7 (3)
C12—C1—C5—O2	−75.2 (2)	C2—O3—C27—O4	−9.8 (3)
O2—C5—C6—C7	179.69 (15)	C2—O3—C27—C21	168.29 (15)
C1—C5—C6—C7	0.5 (3)	C26—C21—C27—O4	−0.4 (3)
C5—C6—C7—C8	−12.7 (3)	C22—C21—C27—O4	−179.8 (2)
C5—C6—C7—C11	−133.0 (2)	C26—C21—C27—O3	−178.48 (17)
C5—C6—C7—C10	108.0 (2)	C22—C21—C27—O3	2.2 (3)

Experimental details

Crystal data
Chemical formula	C₂₃H₂₆O₄
M_r	366.44
Crystal system, space group	Triclinic, P1
Temperature (K)	173
a, b, c (Å)	9.559 (4), 10.201 (5), 11.087 (5)
α, β, γ (°)	69.23 (2), 83.649 (17), 74.823 (17)
V (Å³)	975.4 (8)
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	0.08
Crystal size (mm)	0.45 × 0.40 × 0.20

Data collection
Diffractometer	Nonius KappaCCD diffractometer
Absorption correction	–
No. of measured, independent and observed [I > 2σ(I)] reflections	12665, 3547, 1691
R_int	0.065
(sin θ/λ)_max (Å⁻¹)	0.601

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.043, 0.067, 0.81
No. of reflections	3547
No. of parameters	248
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.17, −0.14

Computer programs: COLLECT (Nonius, 1998), DENZO and SCALEPACK (Otwinowski & Minor, 1997), SHELXS97 (Sheldrick, 2008), SHELXTL-Plus (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008) and PLATON (Spek, 2009).

References

Ciochina, R. & Grossman, R. B. (2006). Chem. Rev. 106, 3963–3986. Web of Science CrossRef PubMed CAS Google Scholar
Nonius (1998). COLLECT. Nonius BV, Delft, The Netherlands. Google Scholar
Otwinowski, Z. & Minor, W. (1997). Methods in Enzymology, Vol. 276, Macromolecular Crystallography, Part A, edited by C. W. Carter Jr & R. M. Sweet, pp. 307–326. New York: Academic Press. Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Spek, A. L. (2009). Acta Cryst. D65, 148–155. Web of Science CrossRef CAS IUCr Journals Google Scholar

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