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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848572Generated: November 3, 2026

Boron tribromide → 3-bromo-4-chloro-N-(2-hydroxy-phenyl)-N-methyl-benzamide

https://huagongshe.com/reaction/1848572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant3-bromo-4-chloro-N-(2-methoxy-phenyl)-N-methyl-benzamideHCID 68602771—
SolventDichloromethaneHCID 6344—
Product3-bromo-4-chloro-N-(2-hydroxy-phenyl)-N-methyl-benzamideHCID 6860311793%

Reaction Steps

To a cooled solution (−70° C.) of 3-bromo-4-chloro-N-(2-methoxy-phenyl)-N-methyl-benzamide (2 g, 5.64 mmol) in DCM (20 mL), BBr3 (1.7 mL, 18 mmol) was added drop-wise over a 20 minute period. The reaction temperature was allowed to increase to room temperature over 12 hrs until completion of the reaction. After concentration in vacuo the mixture was partitioned between DCM and water. 1N NaOH was added to increase pH to ˜5. The organic layer was separated and washed with brine and dried over Na2SO4. Concentration and purification by silica gel column chromatography eluting with hexane/ethyl acetate (4/1 with gradient up to 3/2) yielded 3-bromo-4-chloro-N-(2-hydroxy-phenyl)-N-methyl-benzamide (1.78 g, 93%). MS [M+H]+: 341.9; tR=2.56 min. (method 1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952161B2
Source datasetuspto-grants-2015_02
ORD IDord-47309abad0a84c52a1298edaf421e8bf
Source noteuspto-grants-2015_02