Home Crystal structure of 2-((4-nitrophenyl)thio)ethan-1-ol, C8H9NO3S
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Crystal structure of 2-((4-nitrophenyl)thio)ethan-1-ol, C8H9NO3S

  • Mu-Xuan Lv and Lin-Yan Bian EMAIL logo
Published/Copyright: December 19, 2018

Abstract

C8H9NO3S, triclinic, P1̅ (no. 2), a = 6.984(4) Å, b = 7.494(4) Å, c = 9.174(5) Å, α = 97.249(9)°, β = 95.155(8)°, γ = 108.515(8)°, V = 447.4(4) Å3, Z = 2, Rgt(F) = 0.0538, wRref(F2) = 0.1617, T = 296(2) K.

CCDC no.: 1882283

The asymmetric unit of the title crystal structure is shown in the figure. Tables 1 and 2 contain details on crystal structure and measurement conditions and a list of the atoms including atomic coordinates and displacement parameters.

Source of material

The title compound is synthesized according to the literature known method [3]. In brief, p-nitrochlorobenzene (1.57 g, 10 mmol) and 2-mercapto-ethanol (0.86 g, 11 mmol) were dissolved in DMF (10 mL). NaOH (0.44 g, 11 mmol) was added in portions during a period of 3 h. After then, the reaction mixture was stirred at room temperature for another 2 h, and neutralized by concentrated hydrochloric acid. The evaporation of the solvent and recrystalization of the residue in EtOH/H2O (1:1, v:v) yield yellow plate crystals.

Table 1:

Data collection and handling.

Crystal:Yellow plate
Size:0.20 × 0.20 × 0.06 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.33 mm−1
Diffractometer, scan mode:SMART, φ and ω
θmax, completeness:25.0°, 99%
N(hkl)measured, N(hkl)unique, Rint:2228, 1542, 0.028
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 1369
N(param)refined:119
Programs:SHELX [1], Bruker [2]
Table 2:

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2).

AtomxyzUiso*/Ueq
C10.2852(3)0.1541(3)0.6962(2)0.0433(6)
H1A0.3908930.1055970.7129580.052*
C20.1665(3)0.1680(3)0.8052(2)0.0433(6)
H2A0.1907570.1299680.8957500.052*
C30.0095(3)0.2401(3)0.7776(2)0.0413(6)
H3A0.6011730.1443260.0872390.094*
C4−0.0337(3)0.2908(3)0.6430(3)0.0455(6)
H4A−0.1430520.3343900.6258030.055*
C50.0850(3)0.2767(3)0.5343(2)0.0431(6)
H5A0.0562390.3105330.4427750.052*
C60.2500(3)0.2115(3)0.5608(2)0.0380(5)
C70.3472(3)0.3047(3)0.2843(2)0.0455(6)
H7A0.2125320.2276220.2340380.055*
H7B0.3433640.4299410.3228030.055*
C80.4992(4)0.3222(3)0.1778(3)0.0513(6)
H8A0.4666640.3871570.0989750.062*
H8B0.6347150.3958430.2284980.062*
O1−0.0773(3)0.2127(3)1.0123(2)0.0709(6)
O2−0.2450(3)0.3330(3)0.8710(2)0.0724(6)
O30.4932(3)0.1385(2)0.11832(18)0.0628(6)
N1−0.1122(3)0.2632(3)0.8941(2)0.0490(5)
S10.41818(8)0.19517(8)0.43422(6)0.0474(3)

Experimental details

The structure was solved by direct methods and refined with the SHELX crystallographic software package [1]. The hydrogen atoms were placed at calculated positions and refined as riding atoms with isotropic displacement parameters.

Comment

The p-aminophenyl-β-sulfatoethylsulfone is one of the most important intermediates of vinyl-sulfone reactive dyes [4]. Recently, a novel route for the production of p-aminophenyl-β-sulfatoethylsulfone has been proposed by using p-nitrochlorobenzene as the raw material, and the title compound is the product of the first step of this synthetic protocol [3]. Its crystal structure is presented in this paper.

In the title compound, both the S atom and the nitro group are well conjucted with the central six-membered aryl moiety with the r.m.s. deviation of 0.0360 Å. In the crystal, pairs of intermolecular O—H⋯O hydrogen bonds link two molecules into centrosymmetric dimers. Bond lengths and angles are all in the expected ranges [5].

References

1. Sheldrick, G. M.: Crystal refinement with SHELX. Acta Crystallogr. C71 (2015) 3–8.10.1107/S2053273314026370Search in Google Scholar PubMed PubMed Central

2. BRUKER. SMART and SAINT. Bruker AXS Inc., Madison, WI, (USA) 2007.Search in Google Scholar

3. Tian, Y.; Liu, C.-Y.; Zhang, C.-R.; Wang, W.-B.: Sythesis of p-(β-hydroxylethyl sulfonyl) aniline. Chemical Engineer (China) 189 (2011) 16–18.Search in Google Scholar

4. Feng, X.; Zhang, L.-N.; Chen, H.-Z.: Research progress in synthetic technology of p-aminophenyl-β-sulfatoethylsulfone. Journal of Hebei University of Science and Technology 42 (2017) 256–262.Search in Google Scholar

5. Gessner, V.: Diphenyl[(phenylsulfanyl)methyl]-λ5-phosphanethione. Acta Crystallogr. E70 (2014) o374.10.1107/S1600536814004292Search in Google Scholar PubMed PubMed Central

Received: 2018-10-18
Accepted: 2018-11-30
Published Online: 2018-12-19
Published in Print: 2019-03-26

©2019 Mu-Xuan Lv et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 Public License.

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