Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371712Generated: October 31, 2026

Trichloromethanesulfenyl chloride → HCID 20356001, compound

https://huagongshe.com/reaction/371712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanesulfenyl chlorideHCID 11666—
ReactantSodium HydroxideHCID 14798—
ReactantBicarbamimide, 2-methyl-N-phenyl-HCID 178249—
SolventWaterHCID 962—
ProductHCID 20356001HCID 20356001—

Reaction Steps

To a solution of 38.2g (0.2 mole) 4-phenyl-1-methyl urazole in 200 ml water was added a solution of 8g (0.2 mole) sodium hydroxide in 20 ml water. A mixture of 37.2g (0.2 mole) trichloromethylsulfenyl chloride and 3g of an emulsifier solution (as in example 1) in 25 ml water was then added dropwise to the above basic solution while keeping the reaction mixture at 0° C. The reactants were mixed so that the reaction mixture was kept at a pH greater than 7. The precipitate that formed was filtered and the filter cake washed with water. After drying and recrystallizing from benzene-cyclohexane (1:1, by volume) there was obtained 65g (91%) 4-phenyl-1-methyl-2-(trichloromethylthio) urazole having a melting point of 154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087534
Source datasetuspto-grants-1978_05
ORD IDord-f7138ef1e7504324a24a35a761f7db48
Source noteuspto-grants-1978_05