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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784889Generated: October 30, 2026

Benzyl Bromide → Benzyl 3-benzyloxy-2-nitrobenzoate

https://huagongshe.com/reaction/1784889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Hydroxy-2-nitrobenzoic acidHCID 293291—
SolventDimethylformamideHCID 6228—
ProductBenzyl 3-benzyloxy-2-nitrobenzoateHCID 10594871—

Reaction Steps

3-Hydroxy-2-nitrobenzoic acid (10.5 g) was dissolved in 60 ml of N,N-dimethylformamide, then 15 ml of benzyl bromide and 19.0 g of potassium carbonate were added at 0° C. and the mixture was stirred at room temperature for one night. The reaction solution was filtered through Celite and the filtrate was concentrated in vacuo. Water was added to the resulting residue, the mixture was extracted with ether and the extract was washed with a saturated saline and dried over anhydrous magnesium sulfate. The solvent was evaporated in vacuo to give 20.7 g of benzyl 3-benzyloxy-2-nitrobenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504417B2
Source datasetuspto-grants-2009_03
ORD IDord-7aa221d6ac2744a6922391cd77f30911
Source noteuspto-grants-2009_03