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HRID 1907989생성일: 2026년 10월 26일

2-Aminophenol hydrochloride → 2-(3-Methyl-1-pyrrolyl)phenol

https://huagongshe.com/reaction/1907989

반응식

참여 물질

역할이름HCID투입량
반응물2-Aminophenol hydrochlorideHCID 5800—
반응물Butanedioic acid, 2-methyl-, 1,4-dimethyl esterHCID 15350—
반응물DibahHCID 16682954—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2-(3-Methyl-1-pyrrolyl)phenolHCID 2272344848%

반응 단계

Diisobutylaluminum (100 mL of 1.0 M, 100 mmol) was added dropwise to a solution of dimethyl 2-methylbutanedioate (7.6 g, 48 mmol) in dichloromethane (15 mL) at −78° C., and the solution was stirred for 1 h. A suspension of 2-aminophenol HCl salt (6.6 g, 45 mmol) in water (110 mL) was added initially dropwise with vigorous stirring, then in small portions. About midway through the addition, the cooling bath was removed to help facilitate stirring. The mixture was stirred vigourously at room temperature overnight, then filtered over celite and the filter cake was washed several times with dichloromethane. The filtrate was separated, and the aqueous layer was extracted with dichloromethane (2×20 mL). The combined organics were washed with brine (50 mL), dried over MgSO4, concentrated and purified by column chromatography (0-40% EtOAc/hexane) to give 2-(3-methylpyrrol-1-yl)phenol (3.7 g, 48%) as a yellow oil. ESI-MS m/z calc. 173.2. found 174.3 (M+1)+; Retention time: 1.51 minutes (3 min run).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08598164B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-1df7722d0fc7488282be270e1faa0263
출처 메모uspto-grants-2013_12