Chloroform → HCID 13193332, compound

HRID 1284299Notes

Reaction equation

HRID 1284299 reaction equation
[CH2:1]([S:4]([O:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)(=[O:6])=[O:5])[CH:2]=C.[Cl:14]Cl.[CH:16]([Cl:19])(Cl)Cl>>[Cl:14][CH:2]([CH2:16][Cl:19])[CH2:1][S:4]([O:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)(=[O:6])=[O:5]

Participants

4

Procedure

To a solution of 11.9 g of phenyl 2-propenesulfonate in 80 ml of chloroform was added 7.1 g of chlorine absorbed in 20 ml of chloroform dropwise with stirring below 0°C. After the addition, the mixture was stirred for two hours at room temperature. By distillation of the solvent and fractionation, 22.4 g of phenyl 2,3-dichloropropanesulfonate, B.P. 120°-125°C/0.005 mmHg, was obtained in a yield of 83.3%.

Workup

  1. customabsorbed in 20 ml of chloroform dropwise
  2. additionAfter the addition
  3. stirringthe mixture was stirred for two hours at room temperature
  4. distillationBy distillation of the solvent and fractionation, 22.4 g of phenyl 2,3-dichloropropanesulfonate, B.P. 120°-125°C/0.005 mmHg
  5. customwas obtained in a yield of 83.3%

Sources & evidence

ORD record
ord-756f494b42904707bbda2ec1e90b45e2
Source dataset
uspto-grants-1976_08
Patent number
US03978228

Reaction notes

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