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HRID 1836773생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1836773

반응식

참여 물질

역할이름HCID투입량
반응물2-Phenylisobutyric acidHCID 13222—
반응물4-Chlorobutyryl chlorideHCID 78370—
반응물1-PyrrolidinecarboxamideHCID 138335—
반응물Aluminum(III) ChlorideHCID 6451240—
용매Carbon TetrachlorideHCID 5943—
생성물2-[4-(4-Chloro-butyryl)-phenyl]-2-methyl-propionic acid pyrrolidineamideHCID 6989465078%

반응 단계

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 (6.559, 78%) as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06777555B2
출처 데이터셋uspto-grants-2004_08
ORD IDord-c661aa5fc1944b339fb70ceea8a1b969
출처 메모uspto-grants-2004_08