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HRID 126759作成日:2026年10月26日

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

https://huagongshe.com/reaction/126759

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Trifluoromethyl)phenyl isocyanateHCID 9483—
反応物1-methoxycarbonyl-S-methylisothioureaHCID 293578—
反応物SodiumHCID 5360545—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物3-(3-Trifluoromethylphenyl)-6-methylthio-tetrahydro-1,3,5-triazine-2,4-dioneHCID 7054591586%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04254122
出典データセットuspto-grants-1981_03
ORD IDord-4de95c22b07d4c588c9b466cc74a1852
出典メモuspto-grants-1981_03