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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54192Generated: October 26, 2026

Water → Ethyl 3-bromobenzyloxyacetate

https://huagongshe.com/reaction/54192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl bromoacetateHCID 7748—
Reactant3-Bromobenzyl alcoholHCID 85141—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-bromobenzyloxyacetateHCID 1995832080.5%

Reaction Steps

Part A: 3-Bromobenzyl alcohol (2.0 g) was dissolved in dimethyl formamide (50 ml) in a dry 100 ml flask under nitrogen. Sodium hydride (0.5 g of a 60% suspension in mineral oil, washed with hexane, 11.8 mmol) was added in portions and the mixture was stirred for one hour at room temperature. Ethyl bromoacetate (1.2 ml, 11.8 mmol) was added drop-wise and the reaction was stirred overnight at room temperature then mixed with water (150 ml) and extracted with methylene chloride (3×20 ml). The extracts were combined, washed with water (50 ml), saturated sodium chloride solution (50 ml) and then dried (MgSO4). The solution was filtered and concentrated and the residue was purified by flash chromatography (SiO2, gradient hexane to ethyl acetate) which gave 2.35 g (80%) of ethyl 3-bromobenzyloxyacetate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622937
Source datasetuspto-grants-1997_04
ORD IDord-4ee2eba34d474c2499c65a8ee03e448f
Source noteuspto-grants-1997_04