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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920141Generated: October 30, 2026

Water → 2-Amino-2-(3-bromophenyl)propan-1-ol

https://huagongshe.com/reaction/920141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 2-amino-2-(3-bromophenyl)propanoateHCID 50989094—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-2-(3-bromophenyl)propan-1-olHCID 53256694104.7%

Reaction Conditions

Temperature-7 °C

Reaction Steps

A solution of the (RS)-2-amino-2-(3-bromo-phenyl)-propionic acid methyl ester (9.39 g, 36 mmol) in tetrahydrofuran (360 ml) was treated portionwise at −5° C. with lithiumaluminiumhydride (1.41 g, 36 mmol; 282 mg/2 min). After complete addition, stirring was continued at 0-5° C. for 30 minutes. For the workup, the reaction mixture was cooled to −7° C., and water (9 ml) was added dropwise. Thereafter, 2 N sodium hydroxide solution (9 ml) was added and stirring continued for 15 minutes at room temperature. They grey suspension was filtrated through Dicalite which was washed with tetrahydrofuran (200 ml). The filtrate was evaporated at reduced pressure. There were obtained 8.67 g of crude (RS)-2-amino-2-(3-bromo-phenyl)-propan-1-ol as colorless oil. The purity of the product allowed using it in the next step without further purification. Mass (calculated) C9H12BrNO [230.106]; (found) [M+H]+=230, 232.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273042B2
Source datasetuspto-grants-2016_03
ORD IDord-bac5090afd78423493259680a4828b81
Source noteuspto-grants-2016_03