Bromochloromethane → 1-[(Chloromethyl)sulfanyl]-4-methoxybenzene

HRID 247051Notes

Reaction equation

HRID 247051 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([SH:9])=[CH:5][CH:4]=1.Br[CH2:11][Cl:12].C(N(CC)CC)C>>[Cl:12][CH2:11][S:9][C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1

Participants

4

Procedure

4-Methoxythiophenol (40 mmol) was dissolved in bromochloromethane (0.8 mol) and triethylamine (40 mmol) added dropwise with stirring and external cooling to keep the reaction below room temperature. Once the addition was completed the reaction mixture was stirred at room temperature for 1 h. The mixture was then washed with water, the organic solution dried (MgSO4), the solvent evaporated off and the residue distilled; yield: 3.90 g (52%), b.p. 70° C./0.01 mmHg. The physical data for the title compound are detailed in J. Hayami, N. Tanaka, S. Kurabayashi, Y. Kotani and A. Kaji; Bull.Chem.Soc. (Japan) 44, 3091 (1971).

Workup

  1. temperatureexternal cooling
  2. customthe reaction below room temperature
  3. additionOnce the addition
  4. stirringwas stirred at room temperature for 1 h
  5. washThe mixture was then washed with water
  6. dry with materialthe organic solution dried (MgSO4)
  7. customthe solvent evaporated off
  8. distillationthe residue distilled

Sources & evidence

ORD record
ord-5bd3537b61c34a81a5c136dc0cf73388
Source dataset
uspto-grants-1987_11
Patent number
US04705791

Reaction notes

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