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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833928Generated: October 31, 2026

Chloroform → 1,1'-[(Methanesulfinyl)methylene]bis(4-chlorobenzene)

https://huagongshe.com/reaction/1833928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantPotassium CarbonateHCID 11430—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant1,1'-[(Methylsulfanyl)methylene]bis(4-chlorobenzene)HCID 177077—
SolventWaterHCID 962—
Product1,1'-[(Methanesulfinyl)methylene]bis(4-chlorobenzene)HCID 18249478.2%

Reaction Steps

A solution of 10.7 grams (0.0525 mole) of m-chloroperbenzoic acid in 150 ml. of chloroform was slowly added to a cool solution (5°-7° C.) of 14.1 grams (0.050 mole) of bis(p-chlorophenyl)methyl methyl sulfide in 500 ml. of chloroform, and the resulting solution stirred for two hours at a temperature of 5° C., while a white precipitate formed. The mixture after warming to ambient temperature and holding at this temperature for a two hour period was then mixed with a solution having 20 grams of potassium carbonate in 200 ml. of water. The chloroform phase was then removed and washed with 100 ml. of water, and the chloroform distilled off; the vacuum distillation leaving 14.7 grams of a crude product which was recrystallized twice from 2,2,4-trimethylpentane-benzene (2:1) mixture to yield 11.7 grams (78 percent) of the white colored solid of bis(p-chlorophenyl)methyl methyl sulfoxide with a melting point of 109.5°-110.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04067909
Source datasetuspto-grants-1978_01
ORD IDord-2670513494f14527b77e026a96885a58
Source noteuspto-grants-1978_01