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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595788Generated: November 3, 2026

4-Bromobenzoic acid → (S)-4-bromo-N-(2-hydroxy-1-phenylethyl)benzamide

https://huagongshe.com/reaction/595788

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzoic acidHCID 11464—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-2-phenylethan-1-olHCID 134797—
ReactantPyBroPHCID 2733179—
SolventTetrahydrofuranHCID 8028—
Product(S)-4-bromo-N-(2-hydroxy-1-phenylethyl)benzamideHCID 11335644960%

Reaction Steps

To a solution of 4-bromobenzoic acid (892 mg, 4.44 mmol) in THF (9.9 mL) was added (S)-2-amino-2-phenylethanol (609 mg, 4.44 mmol), DIEA (1.9 mL, 11.1 mmol), PyBroP (2.5 g, 5.32 mmol), and HOBT (815 mg, 5.32 mmol). The reaction mixture was stirred at room temperature for 20 h. The reaction mixture was extracted with EtOAc. The organic layer was washed with water and brine. After dried over anhydrous sodium sulfate, filtered and concentrated in vacuo, the crude product was purified by flash chromatography (gradient EtOAc in DCM) yielding (S)-4-bromo-N-(2-hydroxy-1-phenylethyl)benzamide (850 mg, 60%). LCMS (m/z): 338.1 (MH+), 0.61 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-4f88b6f070cb4ea1a42439300dbb92ce
Source noteuspto-grants-2016_01