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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 126759생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/126759

반응식

참여 물질

역할이름HCID투입량
반응물3-(Trifluoromethyl)phenyl isocyanateHCID 9483—
반응물1-methoxycarbonyl-S-methylisothioureaHCID 293578—
반응물SodiumHCID 5360545—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물3-(3-Trifluoromethylphenyl)-6-methylthio-tetrahydro-1,3,5-triazine-2,4-dioneHCID 7054591586%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04254122
출처 데이터셋uspto-grants-1981_03
ORD IDord-4de95c22b07d4c588c9b466cc74a1852
출처 메모uspto-grants-1981_03