Dimethyl Sulfoxide → 2-Chloro-6-nitro-benzenethiol

HRID 2422440Notes

Reaction equation

HRID 2422440 reaction equation
Cl[C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].C[S:13](C)=O>O>[Cl:8][C:7]1[CH:6]=[CH:5][CH:4]=[C:3]([N+:9]([O-:11])=[O:10])[C:2]=1[SH:13]

Participants

4

Procedure

To a solution of 2,3-dichloronitrobenzene (Aldrich, 19.2 g, 100 mmol) in 300 mL of DMSO was added powdered Na2S 9H2O (Aldrich, 24.0 g, 100 mmol). The mixture was stirred at ambient temperature for 24 h, then was diluted with 2 L of water. The mixture was clarified by filtration and the filtrate was acidified to pH 4 with con. HCl. The mixture was extracted 3× with Et2O (400 mL). The organic layers were combined and washed twice with a brine solution (400 mL), dried over Na2SO4. Removal of the solvent under reduced pressure gave 18.4 g product. 1H NMR (400 MHz, DMSO) δ 8.11 (dd, J=8.3, 1.3 Hz, 1H), 7.93 (dd, J=8.0, 1.3 Hz, 1H), 7.40 (td, J=8.2, 1.3 Hz, 1H) 5.06 (s, 1H). MS (EI): m/z 188 (M−H).

Workup

  1. filtrationThe mixture was clarified by filtration
  2. extractionThe mixture was extracted 3× with Et2O (400 mL)
  3. washwashed twice with a brine solution (400 mL)
  4. dry with materialdried over Na2SO4
  5. customRemoval of the solvent under reduced pressure

Sources & evidence

ORD record
ord-bf2b718b705e43bda47c5400a914a69c
Source dataset
uspto-grants-2011_06
Patent number
US07960408B2

Reaction notes

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