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HRID 1907989作成日:2026年10月25日

2-Aminophenol hydrochloride → HCID 22723448、化合物

https://huagongshe.com/reaction/1907989

反応式

関与物質

役割名称HCID仕込み量
反応物2-Aminophenol hydrochlorideHCID 5800—
反応物Butanedioic acid, 2-methyl-, 1,4-dimethyl esterHCID 15350—
反応物DibahHCID 16682954—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物HCID 22723448HCID 2272344848%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08598164B2
出典データセットuspto-grants-2013_12
ORD IDord-1df7722d0fc7488282be270e1faa0263
出典メモuspto-grants-2013_12