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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19987Generated: October 25, 2026

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

https://huagongshe.com/reaction/19987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methoxy-5-nitrophenolHCID 69471—
SolventAcetoneHCID 180—
Product2-(Benzyloxy)-1-methoxy-4-nitrobenzeneHCID 531403696.5%

Reaction Steps

Potassium carbonate (1.65 gm; 12 mmol) was added to a solution of 2-methoxy-5-nitro phenol (1.69 g; 10 mmol) and benzyl bromide (1.71 gm; 10 mmol) in acetone (60 ml). The reaction mixture was refluxed for 12 hours. The solvent was removed under reduced pressure and the residue was partitioned between ethyl acetate (150 ml) and water (50 ml). The ethyl acetate layer was separated, washed with water (2×50 ml), dried over anhydrous magnesium sulfate. Removal of the solvent under reduced pressure provided 2.5 g of 1-Benzyloxy-2-methoxy-5-nitrobenzene (Yield=96.5%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745490B2
Source datasetuspto-grants-2010_06
ORD IDord-dfb5a266abc740b7aeafad57481660b5
Source noteuspto-grants-2010_06