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HRID 486995作成日:2026年10月24日

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

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

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. Elemental analysis of the product indicated the following:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05292937
出典データセットuspto-grants-1994_03
ORD IDord-c73fa73d58c448baa169fe610b575b16
出典メモuspto-grants-1994_03