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HRID 1724791作成日:2026年10月25日

4-Chlorophenylacetyl chloride → 4-[2-(4-Chloro-phenyl)-acetyl]-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1724791

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chlorophenylacetyl chlorideHCID 90692—
反応物Ethyl 3-methyl-1H-pyrrole-2-carboxylateHCID 5324582—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒1,2-DichloroethaneHCID 11—
溶媒DichloromethaneHCID 6344—
生成物4-[2-(4-Chloro-phenyl)-acetyl]-3-methyl-1H-pyrrole-2-carboxylic acid ethyl esterHCID 57435110—

反応手順

A solution of (4-chlorophenyl)-acetyl chloride (3 mmol) in dichloromethane or 1,2-dichloroethane (4 ml) was added to a solution cooled at −40° C. of 84 (0.229 g, 1.5 mmol) and AlCl3 was added (0.400 g, 3 mmol). The reaction mixture was stirred for 30 minutes at the same temperature. The reaction mixture was poured into ice-water and extracted with ethyl acetate. The organic layer was washed with NaOH (2 M) and brine, dried over Na2SO4, and evaporated to dryness under vacuum to give crude product 85. Crude yield: 96%

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07488747B2
出典データセットuspto-grants-2009_02
ORD IDord-6380e42febbe44d9a6928a7ed799b9d8
出典メモuspto-grants-2009_02