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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129812Generated: October 25, 2026

Trichloromethanesulfenyl chloride → HCID 18788458, compound

https://huagongshe.com/reaction/129812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanesulfenyl chlorideHCID 11666—
ReactantSodium HydroxideHCID 14798—
ReactantMesitylformamidinHCID 18788461—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 18788458HCID 1878845899.1%

Reaction Steps

2.2 g of trichloromethanesulfenyl chloride are introduced into a solution of 2 g of 2,4,6-trimethyl benzamidine in 16 ml of dichloromethane under an inert atmosphere at about -20° C., followed by the slow addition of 2 g of NaOH dissolved in 3.2 ml of water at about -10° C. After I hour at about -5° C., the precipitate formed is isolated and the organic phase is separated and washed with 6 ml of water. After being dried over K2CO3, it is concentrated under reduced pressure to give 2.8 g of the desired product in the form of an oil, which may be used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05470855
Source datasetuspto-grants-1995_11
ORD IDord-80152b1af913426387206ec895462f2e
Source noteuspto-grants-1995_11