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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351887Generated: October 31, 2026

Dimethyl Sulfide → HCID 15631820, compound

https://huagongshe.com/reaction/2351887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantSodium HydroxideHCID 14798—
ReactantChlorosuccinimideHCID 31398—
Reactant2-Bromo-4,5-difluoroanilineHCID 11206558—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 15631820HCID 15631820—

Reaction Steps

To a solution of 2-bromo-4,5-difluoroaniline (100 g) and dimethyl sulfide (49 ml) in anhydrous dichloromethane (1.2 liter) is added gradually N-chlorosuccinimide (90 g) at below 15° C., and thereafter is further added in portions triethylamine (93 ml) at 15° C. After the addition, the mixture is refluxed for 7 hours. After cooling, 10% aqueous sodium hydroxide (one liter) is added to the reaction mixture, and the mixture is extracted with dichloromethane. The extract is dried over magnesium sulfate and concentrated, and the resulting residue is purified by silica gel column chromatography (solvent, dichloromethane:n-hexane=1:2). The product is recrystallized from n-hexane to give 6-bromo-3,4-difluoro-2-methylthiomethylaniline (52 g) as a white crystal, m.p. 60°-61° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874764
Source datasetuspto-grants-1989_10
ORD IDord-136d42fbad774c7aa02e192dd2b65644
Source noteuspto-grants-1989_10