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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378400Generated: October 25, 2026

Triethylamine → 4-Chloro-5-methoxy-6-(methoxymethyl)pyrimidine

https://huagongshe.com/reaction/1378400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178494688HCID 178494688—
Solvent1,1-DichloroethaneHCID 6365—
Product4-Chloro-5-methoxy-6-(methoxymethyl)pyrimidineHCID 15279350—

Reaction Conditions

Temperature80 °C

Reaction Steps

85.0 g (0.5 mol) of 4-hydroxy-5-methoxy-6-methoxymethylpyrimidine were suspended in 600 ml of dichloroethane, 50.5 g of triethylamine were added, and 260 g (1.7 mol) of phosphorus oxychloride were then added without cooling. The mixture was stirred for 3 hours at 80° C., poured into ice-water and neutralized by adding solid sodium carbonate, the organic phase was separated, and the water phase was extracted several times by stirring with methylene chloride. The combined organic phases were dried and concentrated. The residue was distilled under a water pump vacuum. 66.1 g (70% of theory) of a yellow oil were obtained. B.p. 93°-96° C./0.1mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668140
Source datasetuspto-grants-1997_09
ORD IDord-3d4eae15b48d410c83b87577a98525b3
Source noteuspto-grants-1997_09