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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1907989Erstellt: 25. Oktober 2026

2-Aminophenol hydrochloride → HCID 22723448, Verbindung

https://huagongshe.com/reaction/1907989

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Aminophenol hydrochlorideHCID 5800—
EduktButanedioic acid, 2-methyl-, 1,4-dimethyl esterHCID 15350—
EduktDibahHCID 16682954—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 22723448HCID 2272344848%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08598164B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-1df7722d0fc7488282be270e1faa0263
Quellennotizuspto-grants-2013_12