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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623667Generated: November 1, 2026

Benzyl Bromide → Benzyl 2-benzyloxy-5-chlorobenzoate

https://huagongshe.com/reaction/1623667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant5-Chlorosalicylic AcidHCID 9447—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductBenzyl 2-benzyloxy-5-chlorobenzoateHCID 13026912—

Reaction Steps

A mixture of 5-chloro-2-hydroxybenzoic acid (2.03 g, 11.8 mmol), benzyl bromide (2.79 ml, 23.5 mmol) and potassium carbonate (4.87 g, 35.3 mmol) in DMF (20 ml) was stirred at room temperature overnight then heated at 60° C. for 1 hour. Cooled, diluted with water (150 ml) and extracted with ethyl acetate (×3). The organics were washed with water (×2) and brine, dried (MgSO4), and concentrated in vacuo to yield the crude title compound as a yellow oil which was used immediately without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-420922805c514ca59834e9c618b259c7
Source noteuspto-grants-2014_07