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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075155Generated: October 31, 2026

Ethyl bromoacetate → HCID 13306027, compound

https://huagongshe.com/reaction/1075155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Chloro-2(1H)-pyrimidinoneHCID 108578—
SolventEthanolHCID 702—
ProductHCID 13306027HCID 1330602739%

Reaction Steps

5-Chloropyrimid-2-one (0.02 mol) was added to a stirred solution of KOH (0.02 mol) in ethanol (100 ml) followed by addition of ethyl bromoacetate (0.023 mol). The reaction mixture was heated under reflux for 4 h. The reaction mixture was then evaporated to dryness at reduced pressure and the residue was extracted with chloroform (150 ml). The chloroform extract, after filtration, was washed with aqueous 0.5 N NaOH (2×3 ml) and water (3 ml). Evaporation of the dried (MgSO4) solution left the product which was recrystallized from acetone; yield 39%, m.p. 175°-177° C. (Found: C 44.65; H, 4.17. Calc. for C8H9ClN2O3 : C 44.36; H, 4.19).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04395406
Source datasetuspto-grants-1983_07
ORD IDord-35ebdc1f2e5746c8a031698b02e9e95c
Source noteuspto-grants-1983_07