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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 893205생성일: 2026년 10월 25일

Triethylamine → Ethyl 1-(4-chloro-2-ethylphenylaminocarbonyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/893205

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물4-Chloro-2-ethylanilineHCID 34871—
반응물1-(Ethoxycarbonyl)cyclopropanecarboxylic acidHCID 11789472—
용매AcetonitrileHCID 6342—
생성물Ethyl 1-(4-chloro-2-ethylphenylaminocarbonyl)cyclopropanecarboxylateHCID 1909684940%

반응 단계

To a stirred solution of 1.54 grams (0.01 mole) of 1-carboethoxycyclopropanecarboxylic acid (the monocarboxylic acid intermediate described in Example XVIII) and 0.99 gram (0.01 mole) of triethylamine in 75 milliliters of acetonitrile was added a solution of 1.06 grams (0.01 mole) of ethyl chloroformate in 25 milliliters of acetonitrile dropwise with cooling to 0° C.-5° C. After stirring at ice temperature for 30 minutes a solution of 1.52 grams (0.01 mole) of 4-chloro-2-ethylaniline in 20 milliliters of acetonitrile was fed dropwise with stirring and continued cooling. The reaction mixture was allowed to warm to room temperature, then stirred for approximately sixteen hours following which it was filtered and the filtrate freed of solvent by evaporation. The residue was dissolved in dichloromethane and extracted, successively, with water (2×50 milliliters), 2N HCl (2×50 milliliters) and water (1×50 milliliters). After drying (MgSO4), solvent was removed by evaporation and the solid recrystallized from hexane to give 1.15 grams (0.004 mole) of ethyl 1-(4-chloro-2-ethylphenylaminocarbonyl)cyclopropanecarboxylate as cream colored prisms having a melting point of 77° C.-80° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05123951
출처 데이터셋uspto-grants-1992_06
ORD IDord-f370e5f079d2420890f13c7d8f75c678
출처 메모uspto-grants-1992_06