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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398867Generated: November 3, 2026

2,4-Dichloro-6-methyl-5-nitropyrimidine → 4-Chloro-2-methoxy-6-methyl-5-nitropyrimidine

https://huagongshe.com/reaction/1398867

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-6-methyl-5-nitropyrimidineHCID 275294—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-Chloro-2-methoxy-6-methyl-5-nitropyrimidineHCID 1308098025.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium methoxide (28% solution in methanol, 47.0 g, 244 mmol) was added dropwise to a stirred solution of 2,4-dichloro-6-methyl-5-nitropyrimidine (48.3 g, 232 mmol) in methanol (600 mL) at 0° C., and the mixture was stirred at 0° C. for 30 min. The mixture was diluted with water, concentrated, 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 0-15% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the title compound as a yellow solid (11.9 g, 58.5 mmol, 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-b2e50060e1244ab59c44ff4aec67228a
Source noteuspto-grants-2014_12