(E)-3-(3,4-Dimethoxy­phen­yl)-1-(2-thien­yl)prop-2-en-1-one

Fun, H.-K.; Jebas, S.R.; Patil, P.S.; Dharmaprakash, S.M.

doi:10.1107/S1600536808020631

(E)-3-(3,4-Dimethoxyphenyl)-1-(2-thienyl)prop-2-en-1-one

H.-K. Fun, S. R. Jebas, P. S. Patil and S. M. Dharmaprakash

The title compound, C₁₅H₁₄O₃S, has two symmetry-independent molecules in the asymmetric unit with almost identical geometry. The dihedral angle between the benzene and thiophene rings is 1.61 (11)° in one molecule and 7.21 (11)° in the other. In both molecules, C—H

O hydrogen bonds generate rings of graph-set motif S(5). The crystal structure is stabilized by C—H

O hydrogen bonds, C—H

π interactions and π–π interactions involving the benzene and thiophene rings, with centroid–centroid distances of 3.5249 (13) and 3.6057 (13) Å.

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Supporting information

	Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536808020631/ci2626sup1.cif Contains datablocks global, I
	Structure factor file (CIF format) https://doi.org/10.1107/S1600536808020631/ci2626Isup2.hkl Contains datablock I

CCDC reference: 700466

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Key indicators

Single-crystal X-ray study
T = 100 K
Mean (C-C) = 0.003 Å
R factor = 0.060
wR factor = 0.158
Data-to-parameter ratio = 23.0

checkCIF/PLATON results

No syntax errors found



Alert level B
PLAT230_ALERT_2_B Hirshfeld Test Diff for    C2A    --  C3A     ..       8.76 su

Alert level C
PLAT720_ALERT_4_C Number of Unusual/Non-Standard Labels ..........         12

   0 ALERT level A = In general: serious problem
   1 ALERT level B = Potentially serious problem
   1 ALERT level C = Check and explain
   0 ALERT level G = General alerts; check

   0 ALERT type 1 CIF construction/syntax error, inconsistent or missing data
   1 ALERT type 2 Indicator that the structure model may be wrong or deficient
   0 ALERT type 3 Indicator that the structure quality may be low
   1 ALERT type 4 Improvement, methodology, query or suggestion
   0 ALERT type 5 Informative message, check

Comment top

The synthesis and structural studies of chalcone derivatives have been of immense interest because of their biological as well as their increasingly important nonlinear optical properties (Agrinskaya et al., 1999; Chopra et al. 2007). We have previously reported the crystal structures of D–π–A type chalcone derivatives (Patil et al.. 2006; Patil, Ng et al., 2007; Patil, Fun et al., 2007). In continuation of our interest in these compounds, we report herein the crystal structure of the title compound, (I).

There are two independent molecules (A and B) in the asymmetric unit of (I), with similar geometries (Fig. 1). The bond lengths and angles are found to have normal values (Allen et al., 1987). The thiophene rings in both the molecules are planar, with a maximum deviation of 0.002 (3) Å for atom C2A and -0.007 (3) Å for atom C3B. The dihedral angle between the benzene and thiophene rings is 1.61 (11)° in molecule A and 7.21 (11)° in molecule B. In each of the independent molecule, an intramolecular C—H···O hydrogen bond generates an S(5) ring motif (Bernstein et al., 1995).

The crystal structure is consolidated by weak C—H···O and C—H···π interactions (Table 1). The packing is further strengthened by π–π interactions between the S1A/C1A–C4A (centroid Cg1) and C8A–C13A (centroid Cg2) rings [Cg1···Cg2ⁱ = 3.5249 (13) Å] and between the S1B/C1B–C4B (centroid Cg3) and C8B–C13B (centroid Cg4) rings [Cg3···Cg4ⁱⁱ = 3.6057 (13) Å] [symmetry codes: (i) -x, 1-y, -z; (ii) -x, 1-y, -z].

Related literature top

For related literature on the biological and nonlinear optical properties of chalcone derivatives, see: Agrinskaya et al. (1999); Chopra et al. (2007); Patil et al. (2006); Patil, Ng et al. (2007); Patil, Fun et al. (2007). For bond-length data, see: Allen et al. (1987). For graph-set analysis of hydrogen-bond patterns, see: Bernstein et al. (1995).

Experimental top

The title compound was synthesized by the condensation of 3,4-dimethoxybenzaldehyde (0.01 mol, 1.66 g) with 2-acetylthiophene (0.01 mol, 1.07 ml) in methanol (60 ml) in the presence of a catalytic amount of sodium hydroxide solution (5 ml, 30%). After stirring for 6 h, the contents of the flask were poured into ice-cold water (500 ml) and left to stand for 5 h. The resulting crude solid was filtered and dried. The compound was recrystallized from acetone.

Computing details top

Data collection: APEX2 (Bruker, 2005); cell refinement: APEX2 (Bruker, 2005); data reduction: SAINT (Bruker, 2005); program(s) used to solve structure: SHELXTL (Sheldrick, 2008); program(s) used to refine structure: SHELXTL (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2003).

Figures top

	Fig. 1. The asymmetric unit of the title compound, showing 50% probability displacement ellipsoids and the atom-numbering scheme.
	Fig. 2. The crystal packing of the title compound, viewed along the a axis. Hydrogen bonds are shown as dashed lines.

(E)-3-(3,4-Dimethoxyphenyl)-1-(2-thienyl)prop-2-en-1-one top

Crystal data top

C₁₅H₁₄O₃S	F(000) = 1152
M_r = 274.32	D_x = 1.336 Mg m⁻³
Monoclinic, P2₁/n	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2yn	Cell parameters from 3182 reflections
a = 12.1509 (3) Å	θ = 2.3–22.9°
b = 14.3118 (3) Å	µ = 0.24 mm⁻¹
c = 16.3692 (4) Å	T = 100 K
β = 106.570 (2)°	Needle, white
V = 2728.41 (11) Å³	0.60 × 0.17 × 0.11 mm
Z = 8

Data collection top

Bruker SMART APEXII CCD area-detector diffractometer	7997 independent reflections
Radiation source: fine-focus sealed tube	4723 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.074
ϕ and ω scans	θ_max = 30.1°, θ_min = 1.9°
Absorption correction: multi-scan (SADABS; Bruker, 2005)	h = −16→17
T_min = 0.871, T_max = 0.974	k = −20→20
31879 measured reflections	l = −23→23

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)] = 0.060	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.158	H-atom parameters constrained
S = 1.07	w = 1/[σ²(F_o²) + (0.0645P)² + 0.0849P] where P = (F_o² + 2F_c²)/3
7997 reflections	(Δ/σ)_max = 0.001
347 parameters	Δρ_max = 0.46 e Å⁻³
0 restraints	Δρ_min = −0.44 e Å⁻³

Crystal data top

C₁₅H₁₄O₃S	V = 2728.41 (11) Å³
M_r = 274.32	Z = 8
Monoclinic, P2₁/n	Mo Kα radiation
a = 12.1509 (3) Å	µ = 0.24 mm⁻¹
b = 14.3118 (3) Å	T = 100 K
c = 16.3692 (4) Å	0.60 × 0.17 × 0.11 mm
β = 106.570 (2)°

Data collection top

Bruker SMART APEXII CCD area-detector diffractometer	7997 independent reflections
Absorption correction: multi-scan (SADABS; Bruker, 2005)	4723 reflections with I > 2σ(I)
T_min = 0.871, T_max = 0.974	R_int = 0.074
31879 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.060	0 restraints
wR(F²) = 0.158	H-atom parameters constrained
S = 1.07	Δρ_max = 0.46 e Å⁻³
7997 reflections	Δρ_min = −0.44 e Å⁻³
347 parameters

Special details top

Experimental. The data was collected with the Oxford Cyrosystem Cobra low-temperature attachment.

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
S1A	0.30263 (5)	0.34458 (4)	0.21155 (4)	0.03061 (17)
O1A	0.29234 (14)	0.52178 (12)	0.12000 (11)	0.0341 (4)
O2A	−0.29137 (13)	0.76488 (11)	−0.01772 (10)	0.0271 (4)
O3A	−0.23198 (13)	0.90679 (11)	−0.08963 (10)	0.0263 (4)
C1A	0.2263 (2)	0.26572 (18)	0.24872 (16)	0.0347 (6)
H1AA	0.2582	0.2124	0.2787	0.042*
C2A	0.1135 (2)	0.28805 (18)	0.23049 (18)	0.0381 (6)
H2AA	0.0602	0.2516	0.2470	0.046*
C3A	0.08511 (19)	0.37196 (15)	0.18408 (14)	0.0241 (5)
H3AA	0.0117	0.3975	0.1660	0.029*
C4A	0.18303 (19)	0.41151 (16)	0.16895 (14)	0.0254 (5)
C5A	0.1974 (2)	0.49958 (16)	0.12684 (14)	0.0261 (5)
C6A	0.09567 (19)	0.56023 (16)	0.09447 (14)	0.0276 (5)
H6AA	0.0244	0.5411	0.0987	0.033*
C7A	0.1065 (2)	0.64255 (17)	0.05911 (15)	0.0294 (5)
H7AA	0.1800	0.6572	0.0565	0.035*
C8A	0.01813 (19)	0.71264 (17)	0.02396 (14)	0.0273 (5)
C9A	0.0492 (2)	0.79240 (17)	−0.01259 (15)	0.0302 (5)
H9AA	0.1255	0.8011	−0.0114	0.036*
C10A	−0.03157 (19)	0.85911 (17)	−0.05077 (14)	0.0279 (5)
H10A	−0.0096	0.9119	−0.0753	0.034*
C11A	−0.14488 (19)	0.84704 (16)	−0.05229 (13)	0.0241 (5)
C12A	−0.17800 (18)	0.76786 (16)	−0.01398 (14)	0.0228 (5)
C13A	−0.09658 (19)	0.70150 (16)	0.02383 (14)	0.0248 (5)
H13A	−0.1181	0.6492	0.0493	0.030*
C14A	−0.3308 (2)	0.67985 (16)	0.01146 (17)	0.0321 (6)
H14A	−0.4124	0.6830	0.0020	0.048*
H14B	−0.2937	0.6720	0.0712	0.048*
H14C	−0.3127	0.6278	−0.0194	0.048*
C15A	−0.2024 (2)	0.98748 (17)	−0.13146 (16)	0.0323 (6)
H15A	−0.2698	1.0247	−0.1547	0.048*
H15B	−0.1719	0.9677	−0.1766	0.048*
H15C	−0.1459	1.0238	−0.0910	0.048*
S1B	0.37037 (5)	0.38880 (4)	0.72047 (4)	0.03122 (17)
O1B	0.16770 (14)	0.30240 (11)	0.59734 (11)	0.0326 (4)
O2B	−0.10219 (14)	0.60874 (11)	0.21110 (10)	0.0298 (4)
O3B	−0.24951 (13)	0.49172 (11)	0.12281 (10)	0.0307 (4)
C1B	0.45590 (19)	0.48496 (18)	0.73969 (15)	0.0318 (6)
H1BA	0.5199	0.4913	0.7868	0.038*
C2B	0.42056 (19)	0.55139 (17)	0.67877 (15)	0.0293 (5)
H2BA	0.4578	0.6082	0.6791	0.035*
C3B	0.32112 (18)	0.52442 (15)	0.61500 (14)	0.0236 (5)
H3BA	0.2847	0.5621	0.5690	0.028*
C4B	0.28323 (18)	0.43643 (15)	0.62777 (14)	0.0230 (5)
C5B	0.18737 (18)	0.38180 (16)	0.57549 (14)	0.0240 (5)
C6B	0.11733 (18)	0.42482 (16)	0.49650 (14)	0.0240 (5)
H6BA	0.1316	0.4863	0.4842	0.029*
C7B	0.03331 (19)	0.37724 (16)	0.44176 (15)	0.0262 (5)
H7BA	0.0214	0.3165	0.4577	0.031*
C8B	−0.04199 (18)	0.40867 (16)	0.36023 (14)	0.0236 (5)
C9B	−0.12424 (19)	0.34745 (16)	0.31244 (14)	0.0254 (5)
H9BA	−0.1315	0.2884	0.3340	0.030*
C10B	−0.19590 (19)	0.37269 (16)	0.23295 (14)	0.0249 (5)
H10B	−0.2502	0.3307	0.2018	0.030*
C11B	−0.18609 (18)	0.45996 (16)	0.20059 (14)	0.0237 (5)
C12B	−0.10419 (18)	0.52376 (15)	0.24885 (14)	0.0218 (5)
C13B	−0.03375 (18)	0.49828 (16)	0.32695 (14)	0.0231 (5)
H13B	0.0200	0.5406	0.3583	0.028*
C14B	−0.0190 (2)	0.67467 (17)	0.25647 (16)	0.0336 (6)
H14D	−0.0230	0.7300	0.2226	0.050*
H14E	0.0563	0.6478	0.2683	0.050*
H14F	−0.0345	0.6906	0.3091	0.050*
C15B	−0.3363 (2)	0.43030 (18)	0.07416 (16)	0.0374 (6)
H15D	−0.3730	0.4583	0.0199	0.056*
H15E	−0.3923	0.4193	0.1043	0.056*
H15F	−0.3020	0.3720	0.0656	0.056*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
S1A	0.0259 (3)	0.0293 (3)	0.0321 (3)	0.0024 (2)	0.0008 (2)	−0.0001 (3)
O1A	0.0258 (9)	0.0367 (10)	0.0373 (10)	0.0039 (7)	0.0047 (7)	0.0070 (8)
O2A	0.0241 (8)	0.0226 (9)	0.0342 (9)	0.0016 (7)	0.0076 (7)	0.0018 (7)
O3A	0.0254 (8)	0.0255 (9)	0.0270 (9)	0.0027 (7)	0.0060 (7)	0.0050 (7)
C1A	0.0423 (15)	0.0250 (13)	0.0364 (15)	0.0033 (11)	0.0104 (12)	−0.0002 (11)
C2A	0.0387 (15)	0.0299 (15)	0.0513 (17)	−0.0063 (11)	0.0219 (13)	−0.0096 (13)
C3A	0.0225 (11)	0.0194 (12)	0.0285 (12)	0.0018 (9)	0.0041 (9)	−0.0080 (10)
C4A	0.0240 (11)	0.0258 (13)	0.0236 (12)	0.0038 (9)	0.0021 (9)	−0.0081 (10)
C5A	0.0283 (12)	0.0251 (13)	0.0205 (11)	0.0043 (10)	0.0001 (9)	−0.0052 (10)
C6A	0.0247 (11)	0.0285 (14)	0.0261 (12)	0.0042 (10)	0.0015 (9)	−0.0030 (10)
C7A	0.0256 (12)	0.0331 (14)	0.0261 (13)	0.0038 (10)	0.0017 (10)	−0.0016 (11)
C8A	0.0245 (11)	0.0309 (14)	0.0214 (12)	0.0037 (10)	−0.0015 (9)	−0.0015 (10)
C9A	0.0237 (12)	0.0369 (15)	0.0271 (13)	0.0002 (10)	0.0027 (10)	0.0032 (11)
C10A	0.0276 (12)	0.0289 (13)	0.0251 (12)	−0.0016 (10)	0.0040 (10)	0.0036 (10)
C11A	0.0262 (11)	0.0273 (13)	0.0157 (11)	0.0042 (10)	0.0009 (9)	−0.0006 (9)
C12A	0.0229 (11)	0.0249 (12)	0.0203 (11)	0.0015 (9)	0.0054 (9)	−0.0034 (9)
C13A	0.0300 (12)	0.0215 (12)	0.0220 (12)	0.0008 (9)	0.0059 (9)	−0.0002 (9)
C14A	0.0343 (13)	0.0246 (13)	0.0423 (15)	−0.0019 (10)	0.0185 (12)	0.0014 (11)
C15A	0.0313 (13)	0.0298 (14)	0.0351 (14)	0.0028 (10)	0.0082 (11)	0.0120 (11)
S1B	0.0260 (3)	0.0321 (4)	0.0313 (3)	0.0046 (2)	0.0013 (2)	0.0055 (3)
O1B	0.0321 (9)	0.0229 (9)	0.0387 (10)	−0.0015 (7)	0.0036 (8)	0.0055 (8)
O2B	0.0342 (9)	0.0224 (9)	0.0284 (9)	−0.0067 (7)	0.0017 (7)	0.0020 (7)
O3B	0.0332 (9)	0.0256 (9)	0.0260 (9)	−0.0052 (7)	−0.0034 (7)	0.0010 (7)
C1B	0.0221 (11)	0.0390 (15)	0.0312 (13)	0.0035 (10)	0.0027 (10)	−0.0071 (12)
C2B	0.0239 (11)	0.0277 (13)	0.0344 (13)	−0.0022 (10)	0.0054 (10)	−0.0032 (11)
C3B	0.0219 (11)	0.0222 (12)	0.0243 (12)	0.0016 (9)	0.0027 (9)	0.0017 (10)
C4B	0.0227 (11)	0.0224 (12)	0.0233 (12)	0.0032 (9)	0.0058 (9)	−0.0011 (9)
C5B	0.0236 (11)	0.0230 (12)	0.0263 (12)	0.0019 (9)	0.0083 (9)	−0.0018 (10)
C6B	0.0253 (11)	0.0200 (12)	0.0253 (12)	−0.0010 (9)	0.0048 (9)	0.0014 (9)
C7B	0.0263 (12)	0.0198 (12)	0.0315 (13)	0.0013 (9)	0.0068 (10)	0.0034 (10)
C8B	0.0225 (11)	0.0257 (13)	0.0220 (11)	−0.0024 (9)	0.0053 (9)	−0.0029 (9)
C9B	0.0262 (11)	0.0233 (12)	0.0251 (12)	−0.0024 (9)	0.0048 (9)	0.0001 (10)
C10B	0.0240 (11)	0.0211 (12)	0.0274 (12)	−0.0037 (9)	0.0036 (9)	−0.0055 (10)
C11B	0.0229 (11)	0.0239 (12)	0.0218 (11)	0.0003 (9)	0.0025 (9)	−0.0007 (10)
C12B	0.0247 (11)	0.0164 (11)	0.0255 (12)	−0.0007 (9)	0.0091 (9)	0.0014 (9)
C13B	0.0229 (11)	0.0214 (12)	0.0240 (12)	−0.0037 (9)	0.0052 (9)	−0.0041 (9)
C14B	0.0400 (14)	0.0223 (13)	0.0343 (14)	−0.0124 (11)	0.0041 (11)	−0.0027 (11)
C15B	0.0413 (15)	0.0332 (15)	0.0284 (14)	−0.0105 (12)	−0.0051 (11)	0.0002 (11)

Geometric parameters (Å, º) top

S1A—C1A	1.681 (3)	S1B—C1B	1.699 (3)
S1A—C4A	1.714 (2)	S1B—C4B	1.724 (2)
O1A—C5A	1.232 (3)	O1B—C5B	1.235 (3)
O2A—C12A	1.362 (2)	O2B—C12B	1.368 (3)
O2A—C14A	1.439 (3)	O2B—C14B	1.426 (3)
O3A—C11A	1.362 (3)	O3B—C11B	1.364 (3)
O3A—C15A	1.439 (3)	O3B—C15B	1.429 (3)
C1A—C2A	1.355 (3)	C1B—C2B	1.356 (3)
C1A—H1AA	0.93	C1B—H1BA	0.93
C2A—C3A	1.410 (3)	C2B—C3B	1.407 (3)
C2A—H2AA	0.93	C2B—H2BA	0.93
C3A—C4A	1.402 (3)	C3B—C4B	1.377 (3)
C3A—H3AA	0.93	C3B—H3BA	0.93
C4A—C5A	1.471 (3)	C4B—C5B	1.460 (3)
C5A—C6A	1.479 (3)	C5B—C6B	1.466 (3)
C6A—C7A	1.336 (3)	C6B—C7B	1.337 (3)
C6A—H6AA	0.93	C6B—H6BA	0.93
C7A—C8A	1.462 (3)	C7B—C8B	1.457 (3)
C7A—H7AA	0.93	C7B—H7BA	0.93
C8A—C9A	1.390 (3)	C8B—C9B	1.390 (3)
C8A—C13A	1.402 (3)	C8B—C13B	1.408 (3)
C9A—C10A	1.384 (3)	C9B—C10B	1.391 (3)
C9A—H9AA	0.93	C9B—H9BA	0.93
C10A—C11A	1.381 (3)	C10B—C11B	1.375 (3)
C10A—H10A	0.93	C10B—H10B	0.93
C11A—C12A	1.408 (3)	C11B—C12B	1.414 (3)
C12A—C13A	1.384 (3)	C12B—C13B	1.370 (3)
C13A—H13A	0.93	C13B—H13B	0.93
C14A—H14A	0.96	C14B—H14D	0.96
C14A—H14B	0.96	C14B—H14E	0.96
C14A—H14C	0.96	C14B—H14F	0.96
C15A—H15A	0.96	C15B—H15D	0.96
C15A—H15B	0.96	C15B—H15E	0.96
C15A—H15C	0.96	C15B—H15F	0.96

C1A—S1A—C4A	91.80 (12)	C1B—S1B—C4B	91.86 (12)
C12A—O2A—C14A	116.11 (17)	C12B—O2B—C14B	117.02 (18)
C11A—O3A—C15A	116.73 (17)	C11B—O3B—C15B	116.49 (18)
C2A—C1A—S1A	112.9 (2)	C2B—C1B—S1B	112.52 (18)
C2A—C1A—H1AA	123.5	C2B—C1B—H1BA	123.7
S1A—C1A—H1AA	123.5	S1B—C1B—H1BA	123.7
C1A—C2A—C3A	113.4 (2)	C1B—C2B—C3B	112.2 (2)
C1A—C2A—H2AA	123.3	C1B—C2B—H2BA	123.9
C3A—C2A—H2AA	123.3	C3B—C2B—H2BA	123.9
C4A—C3A—C2A	110.4 (2)	C4B—C3B—C2B	113.1 (2)
C4A—C3A—H3AA	124.8	C4B—C3B—H3BA	123.5
C2A—C3A—H3AA	124.8	C2B—C3B—H3BA	123.5
C3A—C4A—C5A	130.5 (2)	C3B—C4B—C5B	130.2 (2)
C3A—C4A—S1A	111.49 (18)	C3B—C4B—S1B	110.32 (17)
C5A—C4A—S1A	118.01 (16)	C5B—C4B—S1B	119.42 (17)
O1A—C5A—C4A	120.2 (2)	O1B—C5B—C4B	120.7 (2)
O1A—C5A—C6A	121.6 (2)	O1B—C5B—C6B	122.0 (2)
C4A—C5A—C6A	118.2 (2)	C4B—C5B—C6B	117.2 (2)
C7A—C6A—C5A	119.8 (2)	C7B—C6B—C5B	121.2 (2)
C7A—C6A—H6AA	120.1	C7B—C6B—H6BA	119.4
C5A—C6A—H6AA	120.1	C5B—C6B—H6BA	119.4
C6A—C7A—C8A	128.6 (2)	C6B—C7B—C8B	128.1 (2)
C6A—C7A—H7AA	115.7	C6B—C7B—H7BA	116.0
C8A—C7A—H7AA	115.7	C8B—C7B—H7BA	116.0
C9A—C8A—C13A	119.0 (2)	C9B—C8B—C13B	118.4 (2)
C9A—C8A—C7A	118.3 (2)	C9B—C8B—C7B	118.9 (2)
C13A—C8A—C7A	122.7 (2)	C13B—C8B—C7B	122.7 (2)
C10A—C9A—C8A	121.1 (2)	C8B—C9B—C10B	121.4 (2)
C10A—C9A—H9AA	119.5	C8B—C9B—H9BA	119.3
C8A—C9A—H9AA	119.5	C10B—C9B—H9BA	119.3
C11A—C10A—C9A	119.8 (2)	C11B—C10B—C9B	119.7 (2)
C11A—C10A—H10A	120.1	C11B—C10B—H10B	120.1
C9A—C10A—H10A	120.1	C9B—C10B—H10B	120.1
O3A—C11A—C10A	124.9 (2)	O3B—C11B—C10B	125.0 (2)
O3A—C11A—C12A	114.88 (19)	O3B—C11B—C12B	115.24 (19)
C10A—C11A—C12A	120.2 (2)	C10B—C11B—C12B	119.7 (2)
O2A—C12A—C13A	125.7 (2)	O2B—C12B—C13B	124.9 (2)
O2A—C12A—C11A	114.77 (19)	O2B—C12B—C11B	114.97 (19)
C13A—C12A—C11A	119.53 (19)	C13B—C12B—C11B	120.2 (2)
C12A—C13A—C8A	120.4 (2)	C12B—C13B—C8B	120.6 (2)
C12A—C13A—H13A	119.8	C12B—C13B—H13B	119.7
C8A—C13A—H13A	119.8	C8B—C13B—H13B	119.7
O2A—C14A—H14A	109.5	O2B—C14B—H14D	109.5
O2A—C14A—H14B	109.5	O2B—C14B—H14E	109.5
H14A—C14A—H14B	109.5	H14D—C14B—H14E	109.5
O2A—C14A—H14C	109.5	O2B—C14B—H14F	109.5
H14A—C14A—H14C	109.5	H14D—C14B—H14F	109.5
H14B—C14A—H14C	109.5	H14E—C14B—H14F	109.5
O3A—C15A—H15A	109.5	O3B—C15B—H15D	109.5
O3A—C15A—H15B	109.5	O3B—C15B—H15E	109.5
H15A—C15A—H15B	109.5	H15D—C15B—H15E	109.5
O3A—C15A—H15C	109.5	O3B—C15B—H15F	109.5
H15A—C15A—H15C	109.5	H15D—C15B—H15F	109.5
H15B—C15A—H15C	109.5	H15E—C15B—H15F	109.5

C4A—S1A—C1A—C2A	−0.2 (2)	C4B—S1B—C1B—C2B	0.18 (19)
S1A—C1A—C2A—C3A	0.3 (3)	S1B—C1B—C2B—C3B	0.5 (3)
C1A—C2A—C3A—C4A	−0.3 (3)	C1B—C2B—C3B—C4B	−1.1 (3)
C2A—C3A—C4A—C5A	−177.2 (2)	C2B—C3B—C4B—C5B	−177.3 (2)
C2A—C3A—C4A—S1A	0.1 (2)	C2B—C3B—C4B—S1B	1.2 (2)
C1A—S1A—C4A—C3A	0.04 (18)	C1B—S1B—C4B—C3B	−0.78 (17)
C1A—S1A—C4A—C5A	177.78 (18)	C1B—S1B—C4B—C5B	177.88 (17)
C3A—C4A—C5A—O1A	−180.0 (2)	C3B—C4B—C5B—O1B	178.9 (2)
S1A—C4A—C5A—O1A	2.8 (3)	S1B—C4B—C5B—O1B	0.6 (3)
C3A—C4A—C5A—C6A	0.8 (3)	C3B—C4B—C5B—C6B	−0.5 (3)
S1A—C4A—C5A—C6A	−176.47 (16)	S1B—C4B—C5B—C6B	−178.83 (15)
O1A—C5A—C6A—C7A	−2.0 (3)	O1B—C5B—C6B—C7B	−4.4 (3)
C4A—C5A—C6A—C7A	177.2 (2)	C4B—C5B—C6B—C7B	175.0 (2)
C5A—C6A—C7A—C8A	−179.6 (2)	C5B—C6B—C7B—C8B	−178.5 (2)
C6A—C7A—C8A—C9A	−177.7 (2)	C6B—C7B—C8B—C9B	179.7 (2)
C6A—C7A—C8A—C13A	0.7 (4)	C6B—C7B—C8B—C13B	0.8 (4)
C13A—C8A—C9A—C10A	−1.7 (3)	C13B—C8B—C9B—C10B	1.1 (3)
C7A—C8A—C9A—C10A	176.7 (2)	C7B—C8B—C9B—C10B	−177.9 (2)
C8A—C9A—C10A—C11A	0.5 (4)	C8B—C9B—C10B—C11B	−0.2 (3)
C15A—O3A—C11A—C10A	1.0 (3)	C15B—O3B—C11B—C10B	3.4 (3)
C15A—O3A—C11A—C12A	−178.46 (19)	C15B—O3B—C11B—C12B	−177.40 (19)
C9A—C10A—C11A—O3A	−178.4 (2)	C9B—C10B—C11B—O3B	178.4 (2)
C9A—C10A—C11A—C12A	1.0 (3)	C9B—C10B—C11B—C12B	−0.8 (3)
C14A—O2A—C12A—C13A	−7.8 (3)	C14B—O2B—C12B—C13B	1.0 (3)
C14A—O2A—C12A—C11A	172.71 (19)	C14B—O2B—C12B—C11B	−178.52 (19)
O3A—C11A—C12A—O2A	−2.1 (3)	O3B—C11B—C12B—O2B	1.3 (3)
C10A—C11A—C12A—O2A	178.4 (2)	C10B—C11B—C12B—O2B	−179.50 (19)
O3A—C11A—C12A—C13A	178.34 (19)	O3B—C11B—C12B—C13B	−178.29 (18)
C10A—C11A—C12A—C13A	−1.1 (3)	C10B—C11B—C12B—C13B	1.0 (3)
O2A—C12A—C13A—C8A	−179.7 (2)	O2B—C12B—C13B—C8B	−179.62 (19)
C11A—C12A—C13A—C8A	−0.2 (3)	C11B—C12B—C13B—C8B	−0.1 (3)
C9A—C8A—C13A—C12A	1.6 (3)	C9B—C8B—C13B—C12B	−0.9 (3)
C7A—C8A—C13A—C12A	−176.8 (2)	C7B—C8B—C13B—C12B	178.1 (2)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C7A—H7AA···O1A	0.93	2.43	2.792 (3)	103
C1B—H1BA···O1Aⁱ	0.93	2.36	3.261 (3)	162
C7B—H7BA···O1B	0.93	2.47	2.816 (3)	102
C14B—H14F···O1Bⁱⁱ	0.96	2.53	3.401 (3)	151
C15A—H15A···Cg1ⁱⁱⁱ	0.96	2.92	3.616 (3)	130
C10A—H10A···Cg3^iv	0.93	2.84	3.636 (3)	144
C3A—H3AA···Cg4	0.93	2.79	3.370 (3)	122

Symmetry codes: (i) −x+1, −y+1, −z+1; (ii) −x, −y+1, −z+1; (iii) x−3/2, −y+1/2, z−3/2; (iv) −x+1/2, y+1/2, −z+1/2.

Experimental details

Crystal data
Chemical formula	C₁₅H₁₄O₃S
M_r	274.32
Crystal system, space group	Monoclinic, P2₁/n
Temperature (K)	100
a, b, c (Å)	12.1509 (3), 14.3118 (3), 16.3692 (4)
β (°)	106.570 (2)
V (Å³)	2728.41 (11)
Z	8
Radiation type	Mo Kα
µ (mm⁻¹)	0.24
Crystal size (mm)	0.60 × 0.17 × 0.11

Data collection
Diffractometer	Bruker SMART APEXII CCD area-detector diffractometer
Absorption correction	Multi-scan (SADABS; Bruker, 2005)
T_min, T_max	0.871, 0.974
No. of measured, independent and observed [I > 2σ(I)] reflections	31879, 7997, 4723
R_int	0.074
(sin θ/λ)_max (Å⁻¹)	0.705

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.060, 0.158, 1.07
No. of reflections	7997
No. of parameters	347
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.46, −0.44

Computer programs: APEX2 (Bruker, 2005), SAINT (Bruker, 2005), SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2003).