戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 343603作成日:2026年10月25日

Triethylamine → 1-Ethyl-3-(2-ethyl-6-isopropylphenyl)-2-thioxo-imidazolin-4-one

https://huagongshe.com/reaction/343603

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Ethyl-6-isopropylphenyl isothiocyanateHCID 144234—
反応物N-EthylglycineHCID 316542—
溶媒ChloroformHCID 6212—
生成物1-Ethyl-3-(2-ethyl-6-isopropylphenyl)-2-thioxo-imidazolin-4-oneHCID 11185387—

反応手順

A mixture of the crude N-ethyl glycine (18.4 g), 2-ethyl-6-isopropylphenyl-isothiocyanate, (20.5 g), triethyl amine (20.2 g) and chloroform (300 mL) was heated at reflux for 6 hours. The solvent was evaporated. The residue was dissolved in ethyl acetate (500 mL) and washed with water (500 mL). The organic phase was evaporated to dryness. The residue was dissolved in ethanol (50 mL), then diluted with diethyl ether (200 mL). The solution was saturated with hydrogen chloride. The mixture was filtered. The solid was discarded. The filtrate was evaporated to dryness. Purification was achieved by flash chromatography on silica gel (5-10% ethyl acetate in hexane). Crystallization from diethyl ether/hexane afforded pure title compound (7.5 g) as a white solid, m.p. 77°-79° C. Anal. Calcd. for. C16H22N2OS: C, 66.17; H, 7.64; N, 9.65. Found: C, 66.12; H, 7.77; N, 9.69. Mass spectrum (EI, M.+) m/z 290.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05861517
出典データセットuspto-grants-1999_01
ORD IDord-1d5a56b47b9343c49c3780fb7af10a54
出典メモuspto-grants-1999_01