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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606460Generated: October 31, 2026

Ethyl bromoacetate → Ethyl (3-cyanophenoxy)acetate

https://huagongshe.com/reaction/606460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant3-CyanophenolHCID 13394—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (3-cyanophenoxy)acetateHCID 24696095101.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

Ethyl bromoacetate (14.7 g, 88.1 mmol) was added dropwise to a suspension of potassium carbonate (12.8 g, 92.3 mmol) and 3-hydroxybenzonitrile (10.0 g, 83.9 mmol) in THF (50 mL) at room temperature, and the mixture was stirred at 50° C. for 24 hr. The mixture was extracted with ethyl acetate and saturated aqueous ammonium chloride solution, and the organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated to give the title compound as a pale-yellow powder (17.5 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915267B2
Source datasetuspto-grants-2011_03
ORD IDord-41c53868d8584131b7fa8886f4ef2b4c
Source noteuspto-grants-2011_03