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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920142Generated: November 1, 2026

Water → (R)-2-amino-2-(5-bromo-2-fluorophenyl)propan-1-ol

https://huagongshe.com/reaction/920142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfateHCID 24436—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant(R)-methyl 2-amino-2-(5-bromo-2-fluorophenyl)propanoateHCID 90015748—
SolventDiethyl EtherHCID 3283—
Product(R)-2-amino-2-(5-bromo-2-fluorophenyl)propan-1-olHCID 5856301090.2%

Reaction Steps

To a solution of (R)-methyl 2-amino-2-(5-bromo-2-fluorophenyl)propanoate (3.95 g, 14.3 mmol, Eq: 1.00) in diethyl ether (120 ml) was added at 0° C. lithium aluminum hydride (652 mg, 17.2 mmol, Eq: 1.2) in five portions. The icebath was removed and stirring continued at room temperature for 2 hours. To the cooled reaction mixture was added dropwise water (652 mg, 652 μl, 36.2 mmol, Eq: 2.53), NaOH (15% in water) (572 mg, 652 μl, 14.3 mmol, Eq: 1.00) and water (1.96 g, 1956 μl, 109 mmol, Eq: 7.59) via syringe (1:1:3 system) and the mixture was stirred for 20 min until a white suspension occurred. Three small spoons of Na2SO4 were added to the mixture, which was filtered after 5 min. The colourless ether solution was evaporated to give (R)-2-amino-2-(5-bromo-2-fluorophenyl)propan-1-ol (3.2 g, 12.9 mmol, 90.2% yield) as a white solid which was used in the next step without further purification. MS (ISP): m/z=248.1 [M+H]+ and 250.0 [M+2+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273042B2
Source datasetuspto-grants-2016_03
ORD IDord-ddfddc17aae74c7986b0f7213fb98beb
Source noteuspto-grants-2016_03