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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485927Generated: November 1, 2026

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

https://huagongshe.com/reaction/1485927

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 numberUS09422310B2
Source datasetuspto-grants-2016_08
ORD IDord-70fb818052bb464892eb513029abe900
Source noteuspto-grants-2016_08