Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810424Generated: October 25, 2026

Benzyl Bromide → Ethyl 2-(4-(benzyloxy)-3-bromophenyl)acetate

https://huagongshe.com/reaction/1810424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
ReactantEthyl 2-(3-bromo-4-hydroxyphenyl)acetateHCID 18620106—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-(4-(benzyloxy)-3-bromophenyl)acetateHCID 18620085—

Reaction Steps

To a suspension of (3-bromo-4-hydroxy-phenyl)-acetic acid ethyl ester (0.100 g, 0.39 mmol) and cesium carbonate (0.376 g, 1.16 mmol) in MeCN was added benzyl bromide (0.06 mL, 0.46 mmol), and the reaction was stirred at room temperature until no starting material was seen by analytical tlc. The mixture was partitioned between EtOAc and H2O, and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, and concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362044B2
Source datasetuspto-grants-2013_01
ORD IDord-9e88770c40fc4e0a91eb52ab3a11bd2a
Source noteuspto-grants-2013_01