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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34792Generated: October 28, 2026

Sodium Hydroxide → 1-Methanesulphonyl-3-(2,2,2-trifluoroethyl)thiourea

https://huagongshe.com/reaction/34792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethanesulfonamideHCID 72879—
Reactant1,1,1-Trifluoro-2-isothiocyanatoethaneHCID 13883777—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product1-Methanesulphonyl-3-(2,2,2-trifluoroethyl)thioureaHCID 2129884319.2%

Reaction Steps

A solution of 2,2,2-trifluoroethylisothiocyanate (1.4 g.) in acetone (20 ml.) was added to a solution of methanesulphonamide (0.95 g.) and sodium hydroxide (0.44 g.) in water (10 ml.) and the mixture stirred and heated under reflux for 18 hours, and then evaporated to dryness. The residue was dissolved in water and the solution washed with ethyl acetate and then acidified with concentrated hydrochloric acid. The mixture was extracted three times with ethyl acetate and the combined extracts dried and evaporated to dryness. The residue was triturated with acetonitrile and filtered and the filtrate evaporated to dryness. The residue was dissolved in ether, and the solution extracted with aqueous sodium bicarbonate solution. The extract was neutralised with N hydrochloric acid and the mixture extracted with ethyl acetate. The ethyl acetate extract was dried and evaporated to dryness to give 1-methanesulphonyl-3-(2,2,2-trifluoroethyl)thiourea (0.45 g.) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04762932
Source datasetuspto-grants-1988_08
ORD IDord-b9627e2ab1d24354b37df860e936bbd0
Source noteuspto-grants-1988_08