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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413436Generated: November 2, 2026

Phosphorus oxychloride → Ethyl 4-chloro-2-ethylpyrimidine-5-carboxylate

https://huagongshe.com/reaction/1413436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178469771HCID 178469771—
SolventTriethylamineHCID 8471—
ProductEthyl 4-chloro-2-ethylpyrimidine-5-carboxylateHCID 12363083—

Reaction Conditions

Temperature0 °C

Reaction Steps

7.5 ml of triethylamine were slowly introduced into 300 ml of phosphorous oxychloride cooled to 0° C., then were added 30 g of 5-ethoxycarbonyl 4-hydroxy 2-ethyl pyrimidine (VII) prepared in the preceding stage and the suspension was brought up to 40° C. under nitrogen scavenging. After dissolution, the phosphorous oxychloride was evaporated and the residue diluted in a mixture of water and chloroform. This was decanted, the chloroform phase was twice washed with water, dried on sodium sulfate and the solvent evaporated. The raw product obtained, after checking the purity by thin layer chromatography, was reacted in the following stage 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04250178
Source datasetuspto-grants-1981_02
ORD IDord-ffd9be3dd206450d9b6d8d96b70394b1
Source noteuspto-grants-1981_02