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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448795Generated: October 31, 2026

Ethyl bromoacetate → HCID 20375653, compound

https://huagongshe.com/reaction/1448795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant3-PhenoxypyridineHCID 200510—
SolventAcetonitrileHCID 6342—
ProductHCID 20375653HCID 20375653—

Reaction Steps

To a solution of 17.1 g of 3-phenoxypyridine [J. Amer. Chem. Soc 59, 297 (1937)] in 100 ml of acetonitrile is added 16.7 g of ethyl bromoacetate and the solution is refluxed for 8 hours. The resulting mixture is concentrated at reduced pressure and the crystalline solid is isolated by filtration to yield 1-(2-ethoxy-2-oxoethyl)-3-phenoxypyridinium bromide; mp 125°-126° C. after recrystallization from acetonitrile-diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04187311
Source datasetuspto-grants-1980_02
ORD IDord-29ebd4fa5934430da8258585cd8ffab2
Source noteuspto-grants-1980_02