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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886888Generated: November 2, 2026

Benzylethanolamine → N-benzyl-6-bromo-2-fluoro-N-(2-hydroxyethyl)benzamide

https://huagongshe.com/reaction/886888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylethanolamineHCID 4348—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-6-fluorobenzoic acidHCID 302621—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventThionyl ChlorideHCID 24386—
ProductN-benzyl-6-bromo-2-fluoro-N-(2-hydroxyethyl)benzamideHCID 6857840997.5%

Reaction Steps

A solution of 6-bromo-2-fluorobenzoic acid (10.0 g, 45.7 mmol) and N,N-dimethylformamide (0.100 ml) in thionylchloride (40 ml) was stirred at 85° C. for 12 hr, and the solvent was evaporated under reduced pressure. The residue was added to a solution of N-benzylethanolamine (6.91 g, 45.7 mmol) and triethylamine (9.55 ml, 68.6 mmol) in tetrahydrofuran (100 ml) under ice-cooling, and the mixture was stirred for 1 hr under ice-cooling and at room temperature for 1 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the desired product (15.7 g, 97.5%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247403B2
Source datasetuspto-grants-2012_08
ORD IDord-b82cc26e824f49f7b8f03f60f8669ead
Source noteuspto-grants-2012_08