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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533251Generated: October 27, 2026

Benzyl Bromide → o-Benzyloxyphenylacetic acid, benzyl ester

https://huagongshe.com/reaction/1533251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Hydroxyphenyl)acetic acidHCID 11970—
SolventDimethylformamideHCID 6228—
Producto-Benzyloxyphenylacetic acid, benzyl esterHCID 56314296.7%

Reaction Steps

To a solution of (2-hydroxyphenyl)acetic acid (125 g) in dimethylformamide (1.9 l) was added potassium carbonate (909 g) and benzyl bromide (281 g) successively. After being stirred for 18 hours, the mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate, washed with 1N aqueous sodium hydroxide solution and brine, dried and evaporated in vacuo. Dichloromethane was added to the residue and the solution was treated with activated carbon. The mixture was filtered and evaporated to give benzyl (2-benzyloxyphenyl)acetate (132 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207686B1
Source datasetuspto-grants-2001_03
ORD IDord-3d17054a086d4b52b171d3986bd2ad16
Source noteuspto-grants-2001_03