Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946901Generated: October 30, 2026

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

https://huagongshe.com/reaction/1946901

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 53256694103.6%

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, 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. MS (ISP): m/z=230.1 [M+H]+, 232.0 [M+2+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399459B2
Source datasetuspto-grants-2013_03
ORD IDord-f505b0729a51410a96554694c167f652
Source noteuspto-grants-2013_03