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HRID 411900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/411900

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US06559312B2
出典データセットuspto-grants-2003_05
ORD IDord-3d4dbb9a732f462c9ef31a4fd3c3f7b6
出典メモuspto-grants-2003_05