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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458669Generated: November 1, 2026

Methanol → Ethyl 2-(6-Chloro-4-pyrimidinyl)acetate

https://huagongshe.com/reaction/1458669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium hydrideHCID 24758—
Reactant4,6-DichloropyrimidineHCID 70943—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-(6-Chloro-4-pyrimidinyl)acetateHCID 54342093—

Reaction Conditions

Temperature50 °C

Reaction Steps

2.7 g (50 mmol) of sodium hydride (80% dispersion in oil) were placed in 100 ml of dry dioxane, and 11.7 g (90 mmol) of ethyl acetoacetate were added dropwise. The mixture was then stirred at 50° C. for 1 hour. After cooling to room temperature, a solution of 4.5 g (30 mmol) of 4,6-dichloropyrimidine in 50 ml of dioxane was added dropwise. After heating at reflux for 6 hours the mixture was cooled to room temperature, 10 ml of methanol were added dropwise in order to destroy superfluous sodium hydride, and the mixture was concentrated. The residue was taken up in water and brought to a pH of 3 to 4 with conc. hydrochloric acid. After extractive stirring with toluene, the organic phase was dried and concentrated. Chromatography on silica gel left 1.8 g (30% of theory) of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852023
Source datasetuspto-grants-1998_12
ORD IDord-d76f463cbef24e9a8eea25876e3b2efc
Source noteuspto-grants-1998_12