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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880472Generated: October 27, 2026

Benzyl Bromide → 2-(Benzyloxy)-1-chloro-4-nitrobenzene

https://huagongshe.com/reaction/880472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-nitrophenolHCID 69264—
SolventAcetoneHCID 180—
Product2-(Benzyloxy)-1-chloro-4-nitrobenzeneHCID 1288193399%

Reaction Steps

Benzyl bromide (0.6 mL, 5.04 mmol) was added dropwise to a mixture of 2-chloro-5-nitro-phenol (800 mg, 4.61 mmol) and potassium carbonate (1.27 g, 9.22 mmol) in acetone (20 mL) at ambient temperature and then heated at reflux for 2 h. The inorganic residue was filtered off and washed with acetone (20 mL). The combined filtrate and washings were concentrated in vacuo and the resulting residue was then dissolved in ethyl acetate (25 mL) and washed successively with water (2×20 mL), brine (20 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to yield 2-benzyloxy-1-chloro-4-nitro-benzene (1.20 g, 99%) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993574B2
Source datasetuspto-grants-2015_03
ORD IDord-7ed985d7eef045f3b58459196320a00d
Source noteuspto-grants-2015_03