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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069873Generated: October 25, 2026

Benzyl Bromide → 2-(Benzyloxy)-1,3-dibromobenzene

https://huagongshe.com/reaction/2069873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-DibromophenolHCID 11847—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-(Benzyloxy)-1,3-dibromobenzeneHCID 1453448999.1%

Reaction Steps

2,6-Dibromophenol (29.30 g, 116 mmol) and benzyl bromide (33.14 g, 194 mmol) were dissolved in 2-butanone (300 mL). Potassium carbonate (29.47 g, 213 mmol) was added, and the mixture was stirred for 1.5 hr at reflux temperature. The reaction mixture was cooled to room temperature, filtered, and evaporated to dryness. The remaining viscous oil was subjected to silicagel column chromatography, flushing with n-pentane to remove benzyl bromide, then DCM/n-pentane=1:1 to elute the product, yielding the product as a white crystalline solid (39.32 g, 99%). 1H-NMR (CDCl3): δ=7.61 (dd, 2H), 7.54 (d, 2H), 7.41 (m, 3H), 6.90 (t, 1H), 5.04, (s, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299202B2
Source datasetuspto-grants-2012_10
ORD IDord-467ddd06c2434f0cbfb6a8b575788b99
Source noteuspto-grants-2012_10