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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925435Generated: October 27, 2026

Boron trifluoride etherate → 2-Amino-2-(3-bromophenyl)propan-1-ol

https://huagongshe.com/reaction/925435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Amino-2-(3-bromophenyl)propanoic acid hydrochlorideHCID 22336992—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-2-(3-bromophenyl)propan-1-olHCID 53256694—

Reaction Steps

NaBH4 (38 g, 1.125 mol) was added at room temperature to a slurry of 2-amino-2-(3-bromo-phenyl)-propionic acid hydrochloride (105 g, 375 mmol) in dry THF. At 0° C. BF3—O(C2H5)2 (158 g, 1.125 mol) was added dropwise. The mixture was allowed to warm to room temperature, stirred for three days, quenched with 1M aqueous NaOH solution, concentrated in vacuo to remove the THF and extracted with EtOAc (3×300 ml). The organic phase was washed with 1M aqueous NaOH solution, dried with sodium sulfate and concentrated in vacuo to yield the title compound, which was used in the next reaction step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284284B2
Source datasetuspto-grants-2016_03
ORD IDord-c561545baadd405fa4c5db447500330b
Source noteuspto-grants-2016_03