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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398952Generated: October 31, 2026

Phosphorus oxychloride → 2-Methoxy-4,6-dimethyl-5-nitropyrimidine

https://huagongshe.com/reaction/1398952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178433502HCID 178433502—
SolventAmmonium ChlorideHCID 25517—
Product2-Methoxy-4,6-dimethyl-5-nitropyrimidineHCID 68737303—

Reaction Conditions

Temperature100 °C

Reaction Steps

4,6-Dimethyl-5-nitropyrimidin-2-ol (18.4 g, 108 mmol) wad added portionwise to a stirred phosphoryl chloride (3.0 mL) at 0° C., and the mixture was stirred at 100° C. for 80 min. The mixture was concentrated in vacuo, and methanol (180 mL) was added to the residue carefully at 0° C. Sodium methoxide (28% solution in methanol, 68.8 g, 357 mmol) was added dropwise to a stirred mixture at 0° C., and the mixture was stirred at 0° C. for 10 min. The mixture was diluted with aqueous saturated ammonium chloride and concentrated in vacuo. The residue was diluted with water and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 5-20% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the title compound as a yellow wax (13.0 g, 71.0 mmol, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-4dfbfb696bcd4357b5f87275abe7e2e8
Source noteuspto-grants-2014_12