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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 399600생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/399600

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N-EthylglycineHCID 316542—
반응물5-Fluoro-o-tolyl IsothiocyanateHCID 519443—
용매ChloroformHCID 6212—
생성물1-Ethyl-3-(5-fluoro-2-methylphenyl)-2-thioxo-imidazolidin-4-oneHCID 1142527241.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05821372
출처 데이터셋uspto-grants-1998_10
ORD IDord-da9371abb57648ee9feeddba89c2fa36
출처 메모uspto-grants-1998_10