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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1266606생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1266606

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 (6.55 g, 78%) as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06548675B2
출처 데이터셋uspto-grants-2003_04
ORD IDord-a583c1583284425a835f13a4ae0c1b44
출처 메모uspto-grants-2003_04