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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247435Generated: October 31, 2026

N-bromobutanimide → 2-(Benzyloxy)-4-bromophenol

https://huagongshe.com/reaction/2247435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-BenzyloxyphenolHCID 80459—
SolventAcetonitrileHCID 6342—
Product2-(Benzyloxy)-4-bromophenolHCID 2187751489.2%

Reaction Steps

12 g of 2-Benzyloxyphenol was dissolved in 300 ml of acetonitrile, 10.7 g of N-bromosuccinimide was added thereto, and the mixture was stirred at room temperature for 2 hours. Additional N-bromosuccinimide (1 g) was added thereto and the mixture was stirred for 1 hour, and further additional N-bromosuccinimide (1 g) was added thereto and the mixture was stirred for 2 hours. The reaction mixture was concentrated, and the residue was diluted with ethyl acetate and washed with water. The organic layer was dried over anhydrous magnesium sulfate and then filtered, and the filtrate was concentrated. The residue was purified by silica gel column chromatography, to give 14.927 g of the title compound in the 10:1 hexane-ethyl acetate fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687664B2
Source datasetuspto-grants-2010_03
ORD IDord-6f3fa34a4b64417d82b21315866600d1
Source noteuspto-grants-2010_03