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HRID 399600作成日:2026年10月25日

Triethylamine → 1-Ethyl-3-(5-fluoro-2-methylphenyl)-2-thioxo-imidazolidin-4-one

https://huagongshe.com/reaction/399600

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物N-EthylglycineHCID 316542—
反応物5-Fluoro-o-tolyl IsothiocyanateHCID 519443—
溶媒ChloroformHCID 6212—
生成物1-Ethyl-3-(5-fluoro-2-methylphenyl)-2-thioxo-imidazolidin-4-oneHCID 1142527241.3%

反応手順

A mixture of the crude N-ethyl glycine (11.5 g), 5-fluoro-2-methylphenyl-isothiocyanate (10.42 g), triethyl amine (12.5 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. The residue was dissolved in diethyl ether (300 mL) and washed with water (200 mL). The organic phase was dried over anhydrous sodium sulfate and evaporated to dryness. Crystallization from ethanol afforded the title compound (6.5 g) as a pink solid, m.p. 98°-100° C. Anal. Calcd. for. C12H13F N2O S: C, 57.13; H, 5.19; N, 11.10. Found: C, 56.88; H, 5.17; N, 11.05. Mass spectrum (EI, M.+) m/z 252.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05821372
出典データセットuspto-grants-1998_10
ORD IDord-da9371abb57648ee9feeddba89c2fa36
出典メモuspto-grants-1998_10