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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126759Generated: October 25, 2026

3-(Trifluoromethyl)phenyl isocyanate → 3-(3-Trifluoromethylphenyl)-6-methylthio-tetrahydro-1,3,5-triazine-2,4-dione

https://huagongshe.com/reaction/126759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenyl isocyanateHCID 9483—
Reactant1-methoxycarbonyl-S-methylisothioureaHCID 293578—
ReactantSodiumHCID 5360545—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product3-(3-Trifluoromethylphenyl)-6-methylthio-tetrahydro-1,3,5-triazine-2,4-dioneHCID 7054591586%

Reaction Steps

Methyl N-[1-(amino)-1-(methylthio)methylene]carbamate (14.8 g.) was dissolved in methylene chloride (150 ml.). 3-Trifluoromethylphenyl isocyanate (18.7 g.) was added to the solution during 5 minutes and the mixture was stirred at room temperature for 2.5 hours. A freshly prepared solution of sodium (2.3 g.) in methanol (20 ml.) was then added during 5 minutes and the subsequent mixture was stirred at room temperature for 16 hours. The mixture was then evaporated and the residue was dissolved in water (400 ml.). The aqueous solution obtained, was extracted with ethyl acetate (2×400 ml.) to remove neutral byproducts, and then acidified with concentrated hydrochloric acid to pH1. The solid which precipitated was separated by filtration, washed with water (3×500 ml.), and dried (over phosphorus pentoxide) to give 3-(3-trifluoromethylphenyl)-6-methylthio-tetrahydro-1,3,5-triazine-2,4-dione (25.9 g., 86%) as a white solid, m.p. 225°-228° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254122
Source datasetuspto-grants-1981_03
ORD IDord-4de95c22b07d4c588c9b466cc74a1852
Source noteuspto-grants-1981_03