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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 64| Part 9| September 2008| Page o1692
doi:10.1107/S1600536808024562

N-(2-Methyl­phen­yl)benzene­sulfonamide

B. Thimme Gowda,a* Sabine Foro,b K. S. Babithaa and Hartmut Fuessb

aDepartment of Chemistry, Mangalore University, Mangalagangotri 574 199, Mangalore, India, and bInstitute of Materials Science, Darmstadt University of Technology, Petersenstrasse 23, D-64287 Darmstadt, Germany
*Correspondence e-mail: gowdabt@yahoo.com

(Received 29 July 2008; accepted 31 July 2008; online 6 August 2008)

In the title compound, C13H13NO2S, the conformation of the N—H bond is anti to the ortho-methyl group on the aniline ring, in contrast to the syn conformation observed with respect to the ortho-chloro group in N-(2-chloro­phen­yl)benzene­sulfonamide. The dihedral angle between the two benzene rings is 61.5 (1)°. Mol­ecules are linked into chains running along the a axis by N—H⋯O hydrogen bonds.

Related literature

For related literature, see: Gelbrich et al., 2007[Gelbrich, T., Hursthouse, M. B. & Threlfall, T. L. (2007). Acta Cryst. B63, 621-632.]; Gowda et al. (2005[Gowda, B. T., Shetty, M. & Jayalakshmi, K. L. (2005). Z. Naturforsch. Teil A, 60, 106-112.], 2007a[Gowda, B. T., Babitha, K. S., Tokarčík, M., Kožíšek, J. & Fuess, H. (2007a). Acta Cryst. E63, o3361.],b[Gowda, B. T., Foro, S. & Fuess, H. (2007b). Acta Cryst. E63, o3325.], 2008[Gowda, B. T., Foro, S., Sowmya, B. P., Nirmala, P. G. & Fuess, H. (2008). Acta Cryst. E64, o1410.]); Perlovich et al. (2006[Perlovich, G. L., Tkachev, V. V., Schaper, K.-J. & Raevsky, O. A. (2006). Acta Cryst. E62, o780-o782.]).

[Scheme 1]

Experimental

Crystal data

  • C13H13NO2S

  • Mr = 247.30

  • Orthorhombic, P 21 21 21

  • a = 6.4840 (6) Å

  • b = 8.6124 (8) Å

  • c = 21.915 (2) Å

  • V = 1223.8 (2) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 0.25 mm−1

  • T = 299 (2) K

  • 0.50 × 0.50 × 0.45 mm
Data collection

  • Oxford Diffraction Xcalibur diffractometer with Sapphire CCD detector

  • Absorption correction: multi-scan (CrysAlis RED; Oxford Diffraction, 2007[Oxford Diffraction (2007). CrysAlis RED. Oxford Diffraction Ltd, Köln, Germany.]) Tmin = 0.884, Tmax = 0.895

  • 4256 measured reflections

  • 2347 independent reflections

  • 2164 reflections with I > 2σ(I)

  • Rint = 0.029
Refinement

  • R[F2 > 2σ(F2)] = 0.039

  • wR(F2) = 0.106

  • S = 1.07

  • 2347 reflections

  • 184 parameters

  • H atoms treated by a mixture of independent and constrained refinement

  • Δρmax = 0.22 e Å−3

  • Δρmin = −0.35 e Å−3

  • Absolute structure: Flack (1983[Flack, H. D. (1983). Acta Cryst. A39, 876-881.]), 883 Friedel pairs

  • Flack parameter: 0.02 (10)

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A D⋯A D—H⋯A
N1—H1N⋯O1i 0.82 (3) 2.11 (3) 2.926 (3) 178 (3)
Symmetry code: (i) [x-{\script{1\over 2}}, -y+{\script{1\over 2}}, -z+1].

Data collection: CrysAlis CCD (Oxford Diffraction, 2004[Oxford Diffraction (2004). CrysAlis CCD. Oxford Diffraction Ltd, Köln, Germany.]); cell refinement: CrysAlis RED (Oxford Diffraction, 2007[Oxford Diffraction (2007). CrysAlis RED. Oxford Diffraction Ltd, Köln, Germany.]); data reduction: CrysAlis RED; 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: PLATON (Spek, 2003[Spek, A. L. (2003). J. Appl. Cryst. 36, 7-13.]); software used to prepare material for publication: SHELXL97.

Supporting information

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536808024562/ci2650sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536808024562/ci2650Isup2.hkl

checkCIF report


Comment top

As part of a study of the substituent effects on the crystal structures of N-(aryl)-sulfonamides the structure of N-(2-methylphenyl)-benzenesulfonamide (N2MPBSA) has been determined (Gowda et al., 2007a,b, 2008). The conformations of the N—H and S═O bonds of the SO2—NH—C group are trans to each other (Fig. 1). Further, the conformation of the N—H bond is anti to the ortho-methyl group in the aniline benzene ring, in contrast to the syn conformation observed with respect to the ortho-chloro group in N-(2-chlorophenyl)-benzenesulfonamide (N2CPBSA) (Perlovich et al., 2006). The two benzene rings are rotated relative to each other by 61.5 (1)° compared to the value of 49.1 (1)° in N2CPBSA. The other bond parameters in N2MPBSA are similar to those in N2CPBSA and other N-(aryl)-sulfonamides (Gelbrich et al., 2007; Gowda et al., 2007a,b, 2008).

In the crystal structure of N2MPBSA (Fig. 1), the molecules are linked into chains running along the a axis by N—H···O hydrogen bonds (Table 1).

Related literature top

For related literature, see: Gelbrich et al., 2007; Gowda et al. (2005, 2007a,b, 2008); Perlovich et al. (2006).

Experimental top

A solution of benzene (10 ml) in chloroform (40 ml) was treated dropwise with chlorosulfonic acid (25 ml) at 273 K. After the initial evolution of hydrogen chloride subsided, the reaction mixture was brought to room temperature and poured into crushed ice in a beaker. The chloroform layer was separated, washed with cold water and allowed to evaporate slowly. The residual benzenesulfonylchloride was treated with o-toluidine in the stoichiometric ratio and boiled for 10 min. The reaction mixture was then cooled to room temperature and added to ice cold water (100 ml). The resultant solid N-(2-methylphenyl)-benzenesulfonamide was filtered under suction and washed thoroughly with cold water. It was then recrystallized to constant melting point from dilute ethanol. The purity of the compound was checked and characterized by recording its infrared and NMR spectra (Gowda et al., 2005). Single crystals of the title compound used for X-ray diffraction studies were grown by slow evaporation of an ethanolic solution at room temperature.

Refinement top

H atoms of the methyl group were positioned geometrically and refined using a riding model, with C-H = 0.96 Å and Uiso(H) = 1.5Ueq(C). The remaining H atoms were located in a difference map and their positional parameters were refined [N-H = 0.82 (3) Å, C-H = 0.88 (4)–1.00 (4) Å] with Uiso(H) = 1.2Ueq(C,N). Three most deviating reflections (0 1 1, 0 1 2, 0 1 3) were omitted from the refinement.

Computing details top

Data collection: CrysAlis CCD (Oxford Diffraction, 2004); cell refinement: CrysAlis RED (Oxford Diffraction, 2007); data reduction: CrysAlis RED (Oxford Diffraction, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: PLATON (Spek, 2003); software used to prepare material for publication: SHELXS97 (Sheldrick, 2008).

Figures top
[Figure 1] Fig. 1. Molecular structure of the title compound, showing the atom labelling scheme. Displacement ellipsoids are drawn at the 50% probability level. H atoms are represented as small spheres of arbitrary radii.
[Figure 2] Fig. 2. Part of the crystal structure of the title compound, viewed down the a axis. Hydrogen bonds are shown as dashed lines.
N-(2-Methylphenyl)benzenesulfonamide top
Crystal data top
C13H13NO2SF(000) = 520
Mr = 247.30Dx = 1.342 Mg m−3
Orthorhombic, P212121Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2ac 2abCell parameters from 2747 reflections
a = 6.4840 (6) Åθ = 2.4–28.0°
b = 8.6124 (8) ŵ = 0.25 mm−1
c = 21.915 (2) ÅT = 299 K
V = 1223.8 (2) Å3Prism, colourless
Z = 40.50 × 0.50 × 0.45 mm
Data collection top
Oxford Diffraction Xcalibur
diffractometer with Sapphire CCD detector		2347 independent reflections
Radiation source: fine-focus sealed tube2164 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.029
ω and ϕ scansθmax = 26.4°, θmin = 3.3°
Absorption correction: multi-scan
(CrysAlis RED; Oxford Diffraction, 2007)		h = −7→5
Tmin = 0.884, Tmax = 0.895k = −10→9
4256 measured reflectionsl = −18→27
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)] = 0.039H atoms treated by a mixture of independent and constrained refinement
wR(F2) = 0.106 w = 1/[σ2(Fo2) + (0.06P)2 + 0.3217P]
where P = (Fo2 + 2Fc2)/3
S = 1.08(Δ/σ)max = 0.014
2347 reflectionsΔρmax = 0.22 e Å−3
184 parametersΔρmin = −0.35 e Å−3
0 restraintsAbsolute structure: Flack (1983), 883 Friedel pairs
Primary atom site location: structure-invariant direct methodsAbsolute structure parameter: 0.02 (10)
Crystal data top
C13H13NO2SV = 1223.8 (2) Å3
Mr = 247.30Z = 4
Orthorhombic, P212121Mo Kα radiation
a = 6.4840 (6) ŵ = 0.25 mm−1
b = 8.6124 (8) ÅT = 299 K
c = 21.915 (2) Å0.50 × 0.50 × 0.45 mm
Data collection top
Oxford Diffraction Xcalibur
diffractometer with Sapphire CCD detector		2347 independent reflections
Absorption correction: multi-scan
(CrysAlis RED; Oxford Diffraction, 2007)		2164 reflections with I > 2σ(I)
Tmin = 0.884, Tmax = 0.895Rint = 0.029
4256 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.039H atoms treated by a mixture of independent and constrained refinement
wR(F2) = 0.106Δρmax = 0.22 e Å−3
S = 1.08Δρmin = −0.35 e Å−3
2347 reflectionsAbsolute structure: Flack (1983), 883 Friedel pairs
184 parametersAbsolute structure parameter: 0.02 (10)
0 restraints
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
xyzUiso*/Ueq
S10.47917 (9)0.38178 (7)0.43612 (2)0.04060 (17)
O10.5270 (3)0.3651 (2)0.49979 (8)0.0608 (5)
O20.6400 (3)0.4082 (2)0.39280 (9)0.0589 (5)
N10.3623 (3)0.2218 (2)0.41762 (8)0.0391 (4)
H1N0.271 (5)0.195 (3)0.4409 (13)0.047*
C10.2996 (3)0.5346 (2)0.43031 (10)0.0362 (5)
C20.3264 (5)0.6510 (3)0.38754 (11)0.0493 (6)
H20.436 (5)0.649 (3)0.3609 (13)0.059*
C30.1819 (6)0.7692 (3)0.38473 (14)0.0617 (8)
H30.199 (5)0.847 (4)0.3560 (15)0.074*
C40.0157 (5)0.7710 (3)0.42368 (14)0.0600 (7)
H4−0.075 (5)0.847 (4)0.4198 (14)0.072*
C5−0.0106 (4)0.6534 (3)0.46522 (13)0.0569 (7)
H5−0.132 (5)0.657 (4)0.4885 (14)0.068*
C60.1308 (4)0.5347 (3)0.46890 (11)0.0462 (6)
H60.111 (5)0.447 (3)0.4956 (12)0.055*
C70.3086 (4)0.1940 (3)0.35437 (10)0.0378 (5)
C80.4396 (4)0.1005 (3)0.31992 (10)0.0455 (5)
C90.3803 (6)0.0680 (4)0.25957 (12)0.0601 (7)
H90.469 (5)0.004 (4)0.2348 (15)0.072*
C100.2019 (6)0.1273 (4)0.23580 (13)0.0689 (9)
H100.181 (5)0.100 (4)0.1956 (16)0.083*
C110.0750 (6)0.2190 (4)0.27027 (14)0.0668 (9)
H11−0.059 (6)0.265 (4)0.2564 (17)0.080*
C120.1286 (4)0.2529 (3)0.33042 (12)0.0522 (6)
H120.043 (5)0.318 (4)0.3561 (14)0.063*
C130.6314 (5)0.0302 (4)0.34651 (15)0.0661 (8)
H13A0.5953−0.03430.38060.079*
H13B0.72220.11140.35990.079*
H13C0.6994−0.03140.31600.079*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
S10.0369 (3)0.0429 (3)0.0419 (3)0.0025 (2)−0.0041 (2)−0.0025 (2)
O10.0723 (13)0.0611 (11)0.0490 (9)0.0122 (11)−0.0249 (9)−0.0039 (8)
O20.0390 (9)0.0623 (12)0.0755 (12)−0.0041 (9)0.0128 (9)−0.0048 (9)
N10.0410 (10)0.0420 (10)0.0342 (9)−0.0013 (9)0.0041 (8)−0.0002 (7)
C10.0388 (11)0.0359 (11)0.0338 (10)0.0002 (9)−0.0040 (9)−0.0036 (9)
C20.0624 (16)0.0477 (14)0.0377 (11)−0.0049 (12)0.0043 (11)0.0037 (10)
C30.090 (2)0.0435 (15)0.0517 (15)0.0008 (15)−0.0140 (15)0.0098 (12)
C40.0627 (17)0.0513 (14)0.0661 (16)0.0170 (14)−0.0170 (15)−0.0092 (12)
C50.0451 (15)0.0594 (16)0.0663 (16)0.0085 (13)0.0036 (13)−0.0143 (12)
C60.0468 (14)0.0462 (14)0.0454 (12)−0.0019 (12)0.0068 (11)−0.0003 (10)
C70.0427 (12)0.0373 (11)0.0333 (10)−0.0047 (9)0.0036 (9)0.0033 (9)
C80.0520 (13)0.0447 (12)0.0398 (11)0.0000 (11)0.0103 (9)0.0012 (10)
C90.081 (2)0.0590 (16)0.0408 (12)−0.0032 (15)0.0152 (14)−0.0044 (12)
C100.095 (2)0.075 (2)0.0368 (12)−0.0140 (19)−0.0078 (15)−0.0007 (14)
C110.068 (2)0.077 (2)0.0549 (16)0.0008 (16)−0.0181 (15)0.0022 (15)
C120.0490 (15)0.0592 (15)0.0484 (13)0.0050 (14)−0.0045 (12)−0.0036 (11)
C130.0553 (17)0.0716 (19)0.0713 (18)0.0198 (16)0.0099 (15)−0.0114 (15)
Geometric parameters (Å, º) top
S1—O21.4284 (19)C6—H60.96 (3)
S1—O11.4365 (17)C7—C121.376 (4)
S1—N11.624 (2)C7—C81.393 (3)
S1—C11.762 (2)C8—C91.405 (4)
N1—C71.449 (3)C8—C131.501 (4)
N1—H1N0.82 (3)C9—C101.368 (5)
C1—C61.383 (3)C9—H90.97 (3)
C1—C21.384 (3)C10—C111.368 (5)
C2—C31.385 (4)C10—H100.92 (3)
C2—H20.92 (3)C11—C121.394 (4)
C3—C41.375 (5)C11—H111.00 (4)
C3—H30.93 (3)C12—H120.97 (3)
C4—C51.373 (4)C13—H13A0.96
C4—H40.88 (4)C13—H13B0.96
C5—C61.376 (4)C13—H13C0.96
C5—H50.94 (3)
O2—S1—O1120.26 (13)C1—C6—H6118.4 (18)
O2—S1—N1108.05 (11)C12—C7—C8121.6 (2)
O1—S1—N1104.97 (11)C12—C7—N1120.5 (2)
O2—S1—C1108.38 (11)C8—C7—N1117.8 (2)
O1—S1—C1106.73 (11)C7—C8—C9117.3 (2)
N1—S1—C1107.90 (10)C7—C8—C13121.9 (2)
C7—N1—S1119.41 (15)C9—C8—C13120.8 (3)
C7—N1—H1N112 (2)C10—C9—C8121.0 (3)
S1—N1—H1N115 (2)C10—C9—H9120.4 (19)
C6—C1—C2120.9 (2)C8—C9—H9118.6 (19)
C6—C1—S1118.63 (17)C11—C10—C9121.0 (3)
C2—C1—S1120.5 (2)C11—C10—H10126 (2)
C1—C2—C3118.5 (3)C9—C10—H10113 (2)
C1—C2—H2120.8 (19)C10—C11—C12119.5 (3)
C3—C2—H2120.7 (19)C10—C11—H11126 (2)
C4—C3—C2120.7 (3)C12—C11—H11115 (2)
C4—C3—H3120 (2)C7—C12—C11119.7 (3)
C2—C3—H3119 (2)C7—C12—H12118.6 (18)
C5—C4—C3120.0 (3)C11—C12—H12121.8 (18)
C5—C4—H4122 (2)C8—C13—H13A109.5
C3—C4—H4118 (2)C8—C13—H13B109.5
C4—C5—C6120.3 (3)H13A—C13—H13B109.5
C4—C5—H5116 (2)C8—C13—H13C109.5
C6—C5—H5123 (2)H13A—C13—H13C109.5
C5—C6—C1119.5 (2)H13B—C13—H13C109.5
C5—C6—H6122.0 (18)
O2—S1—N1—C7−45.0 (2)C2—C1—C6—C5−0.9 (4)
O1—S1—N1—C7−174.43 (18)S1—C1—C6—C5179.7 (2)
C1—S1—N1—C772.0 (2)S1—N1—C7—C12−84.6 (3)
O2—S1—C1—C6−179.00 (18)S1—N1—C7—C898.4 (2)
O1—S1—C1—C6−48.1 (2)C12—C7—C8—C9−0.2 (4)
N1—S1—C1—C664.23 (19)N1—C7—C8—C9176.8 (2)
O2—S1—C1—C21.6 (2)C12—C7—C8—C13−177.3 (3)
O1—S1—C1—C2132.5 (2)N1—C7—C8—C13−0.3 (3)
N1—S1—C1—C2−115.2 (2)C7—C8—C9—C100.6 (4)
C6—C1—C2—C30.9 (4)C13—C8—C9—C10177.7 (3)
S1—C1—C2—C3−179.7 (2)C8—C9—C10—C11−0.6 (5)
C1—C2—C3—C40.2 (4)C9—C10—C11—C120.3 (5)
C2—C3—C4—C5−1.2 (4)C8—C7—C12—C11−0.1 (4)
C3—C4—C5—C61.2 (4)N1—C7—C12—C11−177.1 (3)
C4—C5—C6—C1−0.1 (4)C10—C11—C12—C70.1 (5)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N1—H1N···O1i0.82 (3)2.11 (3)2.926 (3)178 (3)
Symmetry code: (i) x−1/2, −y+1/2, −z+1.

Experimental details

Crystal data
Chemical formulaC13H13NO2S
Mr247.30
Crystal system, space groupOrthorhombic, P212121
Temperature (K)299
a, b, c (Å)6.4840 (6), 8.6124 (8), 21.915 (2)
V (Å3)1223.8 (2)
Z4
Radiation typeMo Kα
µ (mm−1)0.25
Crystal size (mm)0.50 × 0.50 × 0.45
Data collection
DiffractometerOxford Diffraction Xcalibur
diffractometer with Sapphire CCD detector
Absorption correctionMulti-scan
(CrysAlis RED; Oxford Diffraction, 2007)
Tmin, Tmax0.884, 0.895
No. of measured, independent and
observed [I > 2σ(I)] reflections		4256, 2347, 2164
Rint0.029
(sin θ/λ)max (Å−1)0.625
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.039, 0.106, 1.08
No. of reflections2347
No. of parameters184
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å−3)0.22, −0.35
Absolute structureFlack (1983), 883 Friedel pairs
Absolute structure parameter0.02 (10)

Computer programs: CrysAlis CCD (Oxford Diffraction, 2004), CrysAlis RED (Oxford Diffraction, 2007), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), PLATON (Spek, 2003).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N1—H1N···O1i0.82 (3)2.11 (3)2.926 (3)178 (3)
Symmetry code: (i) x−1/2, −y+1/2, −z+1.
 

Acknowledgements

BTG thanks the Alexander von Humboldt Foundation, Bonn, Germany, for extensions of his research fellowship.

References

First citationFlack, H. D. (1983). Acta Cryst. A39, 876–881.  CrossRef CAS Web of Science IUCr Journals Google Scholar
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 First citationGowda, B. T., Foro, S., Sowmya, B. P., Nirmala, P. G. & Fuess, H. (2008). Acta Cryst. E64, o1410.  Web of Science CSD CrossRef IUCr Journals Google Scholar
 First citationGowda, B. T., Shetty, M. & Jayalakshmi, K. L. (2005). Z. Naturforsch. Teil A, 60, 106–112.  CAS Google Scholar
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Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 64| Part 9| September 2008| Page o1692
doi:10.1107/S1600536808024562
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