戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 893205作成日:2026年10月26日

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

https://huagongshe.com/reaction/893205

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物4-Chloro-2-ethylanilineHCID 34871—
反応物1-(Ethoxycarbonyl)cyclopropanecarboxylic acidHCID 11789472—
溶媒AcetonitrileHCID 6342—
生成物Ethyl 1-(4-chloro-2-ethylphenylaminocarbonyl)cyclopropanecarboxylateHCID 1909684940%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05123951
出典データセットuspto-grants-1992_06
ORD IDord-f370e5f079d2420890f13c7d8f75c678
出典メモuspto-grants-1992_06