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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129646Generated: October 26, 2026

Dichloromethane → Trifluoromethyl 1-chloro-N-(p-chlorobenzyl)thioformimidate

https://huagongshe.com/reaction/129646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethanesulfenyl chloride, trifluoro-HCID 67900—
Reactant1-Chloro-4-(isocyanomethyl)benzeneHCID 2757409—
ProductTrifluoromethyl 1-chloro-N-(p-chlorobenzyl)thioformimidateHCID 1893038568%

Reaction Steps

Trifluoromethylsulfenyl chloride (4.0 g, 0.03 mol) is bubbled over 30 minutes into a solution of 4-chlorobenzylisonitrile (3.0 g, 0.02 mol) in methylene chloride, causing the formation of a white precipitate. The suspension is stirred for 16 hours at room temperature and filtered to remove solids. The white filter cake is washed with methylene chloride and solvent is removed under reduced pressure to obtain an amber oil. Bulb-to-bulb distillation of the oil (90°-100° C., 0.05 mmHg) gives the title product as a colorless oil (3.9 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468877
Source datasetuspto-grants-1995_11
ORD IDord-ad5fc0c2af754edcbfdc8a065345f3fb
Source noteuspto-grants-1995_11