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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464680Generated: October 25, 2026

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

https://huagongshe.com/reaction/1464680

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 numberUS05306827
Source datasetuspto-grants-1994_04
ORD IDord-b2e43a961f6743d3b28e2d4174581de4
Source noteuspto-grants-1994_04