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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486995생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/486995

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. Elemental analysis of the product indicated the following:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05292937
출처 데이터셋uspto-grants-1994_03
ORD IDord-c73fa73d58c448baa169fe610b575b16
출처 메모uspto-grants-1994_03