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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156383Generated: November 3, 2026

Dichloromethane → 2-CHLORO-1-(p-t-BUTYLPHENYLSULFONYL)ETHYL PHENYL SULFIDE

https://huagongshe.com/reaction/1156383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-Tert-butyl-4-(ethenesulfonyl)benzeneHCID 879322—
ReactantBenzenesulfenyl chlorideHCID 11008040—
Product2-CHLORO-1-(p-t-BUTYLPHENYLSULFONYL)ETHYL PHENYL SULFIDEHCID 1304480886%

Reaction Steps

To a solution of 21.0 g (93.7 moles) of p-t-butylphenyl vinyl sulfone in 100 ml of methylene chloride at 20° C. was added 14.0 ml (17,5 g, 121 mmoles) of benzenesulfenyl chloride. After 75 minutes the initial red color of the solution had changed to orange. In the same time the temperature of the solution rose to 26° C. After three days at 23° C. the solvent was removed by evaporation. The semicrystalline residue was recrystallized from ethyl acetate-pentane (1:2) to give a first crop of 18.3 g (53%), m.p. 104.0°-105.5° C. and subsequent crops of 8.3 and 3.0 g, for a total yield of 86%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335142
Source datasetuspto-grants-1982_06
ORD IDord-1811a6e43aa7448284219a9a5057e657
Source noteuspto-grants-1982_06