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HRID 1251052作成日:2026年10月25日

2-Phenylisobutyric acid → 2-[4-(4-Chloro-butyryl)-phenyl]-2-methyl-propionic acid pyrrolidineamide

https://huagongshe.com/reaction/1251052

反応式

関与物質

役割名称HCID仕込み量
反応物2-Phenylisobutyric acidHCID 13222—
反応物4-Chlorobutyryl chlorideHCID 78370—
反応物1-PyrrolidinecarboxamideHCID 138335—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒Carbon TetrachlorideHCID 5943—
生成物2-[4-(4-Chloro-butyryl)-phenyl]-2-methyl-propionic acid pyrrolidineamideHCID 6989465078%

反応手順

Add AlCl3 (8.31 g, 62.3 mmol) to carbon tetrachloride (65 mL) under a nitrogen atmosphere at room temperature. Add 4-chlorobutyryl chloride (03.5 mL, 31.2 mmol), stir for 15 minutes and add, by dropwise addition over 15 minutes, a solution of 2-methyl-2-phenyl-propionic acid, pyrrolidineamide (5.64 g, 26.0 mmol) in carbon tetrachloride (60 mL). Stir at room temperature for 17 hours, pour into ice water (100 mL) and separate the layers. Wash the aqueous layer with methylene chloride (2×70 mL), 5% aqueous sodium hydrogen carbonate, combine the organic layers and dry (Na2SO4). Filter, evaporate the filtrate in vacuo and purify by silica gel chromatography (5:2 hexane/ethyl acetate) to give the title compound (6.55 g, 78%) as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06340761B1
出典データセットuspto-grants-2002_01
ORD IDord-41cbc97a93154c90b924d50b5401311b
出典メモuspto-grants-2002_01