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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 3| March 2010| Page o543
doi:10.1107/S1600536810003740

3-(4-Fluoro­phenyl­sulfin­yl)-2,5-di­methyl-1-benzo­furan

Hong Dae Choi,a Pil Ja Seo,a Byeng Wha Sonb and Uk Leeb*

aDepartment of Chemistry, Dongeui University, San 24 Kaya-dong Busanjin-gu, Busan 614-714, Republic of Korea, and bDepartment of Chemistry, Pukyong National University, 599-1 Daeyeon 3-dong, Nam-gu, Busan 608-737, Republic of Korea
*Correspondence e-mail: uklee@pknu.ac.kr

(Received 22 January 2010; accepted 30 January 2010; online 6 February 2010)

In the title compound, C16H13FO2S, the O atom and the 4-fluoro­phenyl group of the 4-fluoro­phenyl­sulfinyl substituent are located on opposite sides of the plane through the benzofuran fragment; the 4-fluoro­phenyl ring is nearly perpendicular to this plane, making a dihedral angle of 87.41 (3). The crystal structure exhibits a weak inter­molecular C—H⋯O hydrogen bond.

Related literature

For the crystal structures of similar 2-methyl-3-phenyl­sulfinyl-1-benzofuran derivatives, see: Choi et al. (2007[Choi, H. D., Seo, P. J., Son, B. W. & Lee, U. (2007). Acta Cryst. E63, o4042.], 2008a[Choi, H. D., Seo, P. J., Son, B. W. & Lee, U. (2008a). Acta Cryst. E64, o1395.],b[Choi, H. D., Seo, P. J., Son, B. W. & Lee, U. (2008b). Acta Cryst. E64, o1476.]). For the pharmacological activity of benzofuran compounds, see: Aslam et al. (2006[Aslam, S. N., Stevenson, P. C., Phythian, S. J., Veitch, N. C. & Hall, D. R. (2006). Tetrahedron, 62, 4214-4226.]); Galal et al. (2009[Galal, S. A., Abd El-All, A. S., Abdallah, M. M. & El-Diwani, H. I. (2009). Bioorg. Med. Chem. Lett. 19, 2420-2428.]); Khan et al. (2005[Khan, M. W., Alam, M. J., Rashid, M. A. & Chowdhury, R. (2005). Bioorg. Med. Chem. 13, 4796-4805.]). For natural products with benzofuran rings, see: Akgul & Anil (2003[Akgul, Y. Y. & Anil, H. (2003). Phytochemistry, 63, 939-943.]); Soekamto et al. (2003[Soekamto, N. H., Achmad, S. A., Ghisalberti, E. L., Hakim, E. H. & Syah, Y. M. (2003). Phytochemistry, 64, 831-834.]).

[Scheme 1]

Experimental

Crystal data

  • C16H13FO2S

  • Mr = 288.32

  • Monoclinic, P 21 /c

  • a = 11.3951 (5) Å

  • b = 6.1223 (3) Å

  • c = 19.6899 (9) Å

  • β = 100.155 (2)°

  • V = 1352.13 (11) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 0.25 mm−1

  • T = 173 K

  • 0.30 × 0.30 × 0.21 mm
Data collection

  • Bruker SMART APEXII CCD diffractometer

  • Absorption correction: multi-scan (SADABS; Bruker, 2009[Bruker (2009). SADABS. APEX2 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.]) Tmin = 0.645, Tmax = 0.746

  • 22996 measured reflections

  • 3115 independent reflections

  • 2830 reflections with I > 2σ(I)

  • Rint = 0.032
Refinement

  • R[F2 > 2σ(F2)] = 0.035

  • wR(F2) = 0.099

  • S = 1.07

  • 3115 reflections

  • 183 parameters

  • H-atom parameters constrained

  • Δρmax = 0.30 e Å−3

  • Δρmin = −0.32 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A D⋯A D—H⋯A
C10—H10B⋯O2i 0.98 2.62 3.554 (2) 159
Symmetry code: (i) [-x+2, y+{\script{1\over 2}}, -z+{\script{3\over 2}}].

Data collection: APEX2 (Bruker, 2009[Bruker (2009). SADABS. APEX2 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.]); cell refinement: SAINT (Bruker, 2009[Bruker (2009). SADABS. APEX2 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.]); data reduction: SAINT; 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: ORTEP-3 (Farrugia, 1997[Farrugia, L. J. (1997). J. Appl. Cryst. 30, 565.]) and DIAMOND (Brandenburg, 1998[Brandenburg, K. (1998). DIAMOND. Crystal Impact GbR, Bonn, Germany.]); software used to prepare material for publication: SHELXL97.

Supporting information

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536810003740/fk2012sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536810003740/fk2012Isup2.hkl

checkCIF report


Comment top

Molecules containing benzofuran skeleton show various pharmacological activities such as antifungal (Aslam et al., 2006), antitumor and antiviral (Galal et al., 2009), antimicrobial (Khan et al., 2005) properties, and these compounds are widely occurring in nature (Akgul & Anil, 2003; Soekamto et al., 2003). As a part of our ongoing studies of the effect of side chain substituents on the solid state structures of 2-methyl-3-phenylsulfinyl-1-benzofuran analogues (Choi et al., 2007, 2008a,b), we report the crystal structure of the title compound (Fig. 1).

The benzofuran unit is essentially planar, with a mean deviation of 0.009 (1) ° from the least-squares plane defined by the nine constituent atoms. The 4-fluorophenyl ring is almost perpendicular to the plane of the benzofuran fragment [87.41 (3)°] and is tilted slightly towards it. The crystal packing (Fig. 2) is stabilized by a weak intermolecular C—H···O hydrogen bond between the methyl H atom and the oxygen of the S═O unit, with a C10—H10B···O2i (Table 1).

Related literature top

For the crystal structures of similar 2-methyl-3-phenylsulfinyl-1-benzofuran derivatives, see: Choi et al. (2007, 2008a,b). For the pharmacological activity of benzofuran compounds, see: Aslam et al. (2006); Galal et al. (2009); Khan et al. (2005). For natural products with benzofuran rings, see: Akgul & Anil (2003); Soekamto et al. (2003).

Experimental top

77% 3-Chloroperoxybenzoic acid (291 mg, 1.3 mmol) was added in small portions to a stirred solution of 3-(4-fluorophenylsulfanyl)-2,5-dimethyl-1-benzofuran (326 mg, 1.2 mmol) in dichloromethane (30 mL) at 273 K. After being stirred at room temperature for 3h, the mixture was washed with saturated sodium bicarbonate solution and the organic layer was separated, dried over magnesium sulfate, filtered and concentrated in vacuum. The residue was purified by column chromatography (hexane-ethyl acetate, 1:1 v/v) to afford the title compound as a colorless solid [yield 80%, m.p. 420-421 K; Rf = 0.69 (hexane-ethyl acetate, 1:1 v/v)]. Single crystals suitable for X-ray diffraction were prepared by slow evaporation of a solution of the title compound in ethyl acetate at room temperature.

Refinement top

All H atoms were positioned geometrically and refined using a riding model, with C–H = 0.95 Å for aryl and 0.98 Å for methyl H atoms. Uiso(H) = 1.2Ueq (C) for aryl and 1.5Ueq(C) for methyl H atoms.

Computing details top

Data collection: APEX2 (Bruker, 2009); cell refinement: SAINT (Bruker, 2009); data reduction: SAINT (Bruker, 2009); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 (Farrugia, 1997) and DIAMOND (Brandenburg, 1998); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008).

Figures top
[Figure 1] Fig. 1. The molecular structure of the title compound with the atom numbering scheme. Displacement ellipsoids are drawn at the 50 % probability level. H atoms are presented as a small spheres of arbitrary radius.
[Figure 2] Fig. 2. C–H···O interaction (dotted lines) in the crystal structure of the title compound. [Symmetry codes: (i) - x + 2, y + 1/2, - z + 3/2; (ii) - x + 2, y - 1/2, - z + 3/2.]
3-(4-Fluorophenylsulfinyl)-2,5-dimethyl-1-benzofuran top
Crystal data top
C16H13FO2SF(000) = 600
Mr = 288.32Dx = 1.416 Mg m−3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybcCell parameters from 9959 reflections
a = 11.3951 (5) Åθ = 2.5–27.6°
b = 6.1223 (3) ŵ = 0.25 mm−1
c = 19.6899 (9) ÅT = 173 K
β = 100.155 (2)°Block, colourless
V = 1352.13 (11) Å30.30 × 0.30 × 0.21 mm
Z = 4
Data collection top
Bruker SMART APEXII CCD
diffractometer		3115 independent reflections
Radiation source: Rotating Anode2830 reflections with I > 2σ(I)
Bruker HELIOS graded multilayer optics monochromatorRint = 0.032
Detector resolution: 10.0 pixels mm-1θmax = 27.6°, θmin = 1.8°
ϕ and ω scansh = −14→14
Absorption correction: multi-scan
(SADABS; Bruker, 2009)		k = −7→7
Tmin = 0.645, Tmax = 0.746l = −25→25
22996 measured reflections
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.035Hydrogen site location: difference Fourier map
wR(F2) = 0.099H-atom parameters constrained
S = 1.07 w = 1/[σ2(Fo2) + (0.0508P)2 + 0.5136P]
where P = (Fo2 + 2Fc2)/3
3115 reflections(Δ/σ)max < 0.001
183 parametersΔρmax = 0.30 e Å−3
0 restraintsΔρmin = −0.32 e Å−3
Crystal data top
C16H13FO2SV = 1352.13 (11) Å3
Mr = 288.32Z = 4
Monoclinic, P21/cMo Kα radiation
a = 11.3951 (5) ŵ = 0.25 mm−1
b = 6.1223 (3) ÅT = 173 K
c = 19.6899 (9) Å0.30 × 0.30 × 0.21 mm
β = 100.155 (2)°
Data collection top
Bruker SMART APEXII CCD
diffractometer		3115 independent reflections
Absorption correction: multi-scan
(SADABS; Bruker, 2009)		2830 reflections with I > 2σ(I)
Tmin = 0.645, Tmax = 0.746Rint = 0.032
22996 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0350 restraints
wR(F2) = 0.099H-atom parameters constrained
S = 1.07Δρmax = 0.30 e Å−3
3115 reflectionsΔρmin = −0.32 e Å−3
183 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 > 2sigma(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
S0.93298 (3)0.31885 (6)0.605178 (18)0.03074 (12)
F10.72777 (10)0.51180 (19)0.31715 (5)0.0556 (3)
O10.68994 (9)0.46191 (17)0.71689 (5)0.0346 (2)
O20.96804 (10)0.08380 (18)0.60734 (6)0.0410 (3)
C10.80592 (12)0.3425 (2)0.64361 (7)0.0277 (3)
C20.70234 (11)0.2027 (2)0.63519 (7)0.0262 (3)
C30.66200 (12)0.0220 (2)0.59513 (7)0.0299 (3)
H30.7071−0.03420.56280.036*
C40.55514 (12)−0.0758 (2)0.60278 (7)0.0320 (3)
C50.48975 (13)0.0120 (3)0.65052 (7)0.0358 (3)
H50.4167−0.05560.65540.043*
C60.52732 (13)0.1926 (3)0.69067 (8)0.0369 (3)
H60.48200.25080.72250.044*
C70.63433 (12)0.2835 (2)0.68184 (7)0.0291 (3)
C80.79456 (12)0.4921 (2)0.69286 (7)0.0310 (3)
C90.51060 (15)−0.2747 (3)0.56091 (9)0.0433 (4)
H9A0.5564−0.29370.52360.065*
H9B0.4260−0.25580.54120.065*
H9C0.5204−0.40410.59070.065*
C100.87069 (16)0.6753 (3)0.72348 (8)0.0419 (4)
H10A0.94210.68300.70220.063*
H10B0.89420.65180.77330.063*
H10C0.82620.81260.71530.063*
C110.86493 (11)0.3744 (2)0.51764 (7)0.0266 (3)
C120.86759 (12)0.2162 (2)0.46786 (7)0.0305 (3)
H120.90080.07650.48040.037*
C130.82143 (13)0.2629 (3)0.39942 (8)0.0355 (3)
H130.82270.15680.36440.043*
C140.77397 (13)0.4659 (3)0.38377 (8)0.0364 (3)
C150.77240 (14)0.6277 (3)0.43241 (9)0.0391 (3)
H150.73920.76720.41960.047*
C160.82041 (13)0.5810 (2)0.50024 (8)0.0348 (3)
H160.82280.69010.53480.042*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
S0.02162 (18)0.0348 (2)0.0361 (2)0.00162 (12)0.00577 (13)−0.00400 (13)
F10.0606 (6)0.0669 (7)0.0382 (5)0.0008 (5)0.0062 (5)0.0120 (5)
O10.0392 (5)0.0384 (5)0.0284 (5)−0.0003 (4)0.0118 (4)−0.0062 (4)
O20.0384 (6)0.0412 (6)0.0443 (6)0.0170 (5)0.0095 (5)0.0035 (5)
C10.0259 (6)0.0283 (6)0.0291 (6)0.0017 (5)0.0055 (5)−0.0020 (5)
C20.0242 (6)0.0276 (6)0.0271 (6)0.0043 (5)0.0051 (5)0.0031 (5)
C30.0277 (6)0.0284 (6)0.0341 (7)0.0034 (5)0.0072 (5)−0.0016 (5)
C40.0297 (7)0.0301 (7)0.0348 (7)0.0004 (5)0.0021 (5)0.0047 (5)
C50.0285 (7)0.0438 (8)0.0358 (7)−0.0036 (6)0.0076 (6)0.0081 (6)
C60.0342 (8)0.0477 (9)0.0319 (7)0.0024 (6)0.0140 (6)0.0021 (6)
C70.0319 (7)0.0316 (7)0.0245 (6)0.0029 (5)0.0064 (5)0.0007 (5)
C80.0327 (7)0.0332 (7)0.0270 (6)0.0017 (5)0.0045 (5)−0.0007 (5)
C90.0394 (8)0.0358 (8)0.0532 (9)−0.0082 (6)0.0044 (7)−0.0019 (7)
C100.0495 (9)0.0397 (8)0.0359 (8)−0.0069 (7)0.0057 (7)−0.0108 (6)
C110.0204 (6)0.0265 (6)0.0350 (7)−0.0017 (5)0.0106 (5)−0.0012 (5)
C120.0256 (6)0.0258 (6)0.0414 (7)0.0004 (5)0.0090 (5)−0.0041 (5)
C130.0312 (7)0.0388 (7)0.0381 (8)−0.0038 (6)0.0110 (6)−0.0091 (6)
C140.0309 (7)0.0432 (8)0.0364 (7)−0.0050 (6)0.0097 (6)0.0058 (6)
C150.0397 (8)0.0295 (7)0.0497 (9)0.0032 (6)0.0125 (7)0.0077 (6)
C160.0362 (7)0.0269 (7)0.0436 (8)0.0026 (5)0.0135 (6)−0.0036 (6)
Geometric parameters (Å, º) top
S—O21.4921 (11)C8—C101.480 (2)
S—C11.7540 (13)C9—H9A0.9800
S—C111.7935 (14)C9—H9B0.9800
F1—C141.3540 (18)C9—H9C0.9800
O1—C81.3705 (17)C10—H10A0.9800
O1—C71.3846 (17)C10—H10B0.9800
C1—C81.3567 (18)C10—H10C0.9800
C1—C21.4434 (18)C11—C121.3824 (19)
C2—C31.3892 (19)C11—C161.3830 (19)
C2—C71.3927 (18)C12—C131.387 (2)
C3—C41.3886 (19)C12—H120.9500
C3—H30.9500C13—C141.369 (2)
C4—C51.405 (2)C13—H130.9500
C4—C91.508 (2)C14—C151.380 (2)
C5—C61.383 (2)C15—C161.381 (2)
C5—H50.9500C15—H150.9500
C6—C71.379 (2)C16—H160.9500
C6—H60.9500
O2—S—C1107.72 (7)C4—C9—H9B109.5
O2—S—C11106.18 (6)H9A—C9—H9B109.5
C1—S—C1198.57 (6)C4—C9—H9C109.5
C8—O1—C7106.49 (10)H9A—C9—H9C109.5
C8—C1—C2107.65 (12)H9B—C9—H9C109.5
C8—C1—S123.65 (11)C8—C10—H10A109.5
C2—C1—S128.47 (10)C8—C10—H10B109.5
C3—C2—C7119.36 (12)H10A—C10—H10B109.5
C3—C2—C1136.00 (12)C8—C10—H10C109.5
C7—C2—C1104.64 (12)H10A—C10—H10C109.5
C4—C3—C2119.37 (12)H10B—C10—H10C109.5
C4—C3—H3120.3C12—C11—C16121.21 (13)
C2—C3—H3120.3C12—C11—S119.25 (10)
C3—C4—C5119.09 (13)C16—C11—S119.29 (11)
C3—C4—C9120.40 (13)C11—C12—C13119.50 (13)
C5—C4—C9120.50 (13)C11—C12—H12120.2
C6—C5—C4122.76 (13)C13—C12—H12120.2
C6—C5—H5118.6C14—C13—C12118.22 (13)
C4—C5—H5118.6C14—C13—H13120.9
C7—C6—C5116.24 (13)C12—C13—H13120.9
C7—C6—H6121.9F1—C14—C13118.51 (14)
C5—C6—H6121.9F1—C14—C15118.21 (14)
C6—C7—O1126.34 (12)C13—C14—C15123.27 (14)
C6—C7—C2123.18 (13)C14—C15—C16118.09 (14)
O1—C7—C2110.48 (12)C14—C15—H15121.0
C1—C8—O1110.74 (12)C16—C15—H15121.0
C1—C8—C10132.86 (14)C15—C16—C11119.64 (14)
O1—C8—C10116.40 (12)C15—C16—H16120.2
C4—C9—H9A109.5C11—C16—H16120.2
O2—S—C1—C8131.07 (12)C1—C2—C7—O10.42 (14)
C11—S—C1—C8−118.80 (12)C2—C1—C8—O1−0.67 (16)
O2—S—C1—C2−42.67 (14)S—C1—C8—O1−175.53 (9)
C11—S—C1—C267.46 (13)C2—C1—C8—C10−179.96 (15)
C8—C1—C2—C3−178.80 (15)S—C1—C8—C105.2 (2)
S—C1—C2—C3−4.3 (2)C7—O1—C8—C10.92 (15)
C8—C1—C2—C70.15 (15)C7—O1—C8—C10−179.66 (12)
S—C1—C2—C7174.69 (10)O2—S—C11—C12−7.30 (12)
C7—C2—C3—C4−0.5 (2)C1—S—C11—C12−118.67 (11)
C1—C2—C3—C4178.31 (14)O2—S—C11—C16178.43 (11)
C2—C3—C4—C50.6 (2)C1—S—C11—C1667.07 (12)
C2—C3—C4—C9−178.81 (13)C16—C11—C12—C13−2.0 (2)
C3—C4—C5—C6−0.1 (2)S—C11—C12—C13−176.18 (10)
C9—C4—C5—C6179.28 (14)C11—C12—C13—C14−0.3 (2)
C4—C5—C6—C7−0.4 (2)C12—C13—C14—F1−179.40 (12)
C5—C6—C7—O1−179.06 (13)C12—C13—C14—C151.6 (2)
C5—C6—C7—C20.5 (2)F1—C14—C15—C16−179.50 (13)
C8—O1—C7—C6178.76 (14)C13—C14—C15—C16−0.5 (2)
C8—O1—C7—C2−0.82 (15)C14—C15—C16—C11−1.9 (2)
C3—C2—C7—C60.0 (2)C12—C11—C16—C153.1 (2)
C1—C2—C7—C6−179.18 (13)S—C11—C16—C15177.30 (11)
C3—C2—C7—O1179.58 (11)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
C10—H10B···O2i0.982.623.554 (2)159
Symmetry code: (i) −x+2, y+1/2, −z+3/2.

Experimental details

Crystal data
Chemical formulaC16H13FO2S
Mr288.32
Crystal system, space groupMonoclinic, P21/c
Temperature (K)173
a, b, c (Å)11.3951 (5), 6.1223 (3), 19.6899 (9)
β (°) 100.155 (2)
V (Å3)1352.13 (11)
Z4
Radiation typeMo Kα
µ (mm−1)0.25
Crystal size (mm)0.30 × 0.30 × 0.21
Data collection
DiffractometerBruker SMART APEXII CCD
diffractometer
Absorption correctionMulti-scan
(SADABS; Bruker, 2009)
Tmin, Tmax0.645, 0.746
No. of measured, independent and
observed [I > 2σ(I)] reflections		22996, 3115, 2830
Rint0.032
(sin θ/λ)max (Å−1)0.651
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.035, 0.099, 1.07
No. of reflections3115
No. of parameters183
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å−3)0.30, −0.32

Computer programs: APEX2 (Bruker, 2009), SAINT (Bruker, 2009), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 (Farrugia, 1997) and DIAMOND (Brandenburg, 1998).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
C10—H10B···O2i0.982.623.554 (2)159.4
Symmetry code: (i) −x+2, y+1/2, −z+3/2.
 

References

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ISSN: 2056-9890
Volume 66| Part 3| March 2010| Page o543
doi:10.1107/S1600536810003740
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