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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628511Generated: October 31, 2026

4-Chloro-2-methoxy-6-methyl-5-nitropyrimidine → 2-Methoxy-4,6-dimethyl-5-nitropyrimidine

https://huagongshe.com/reaction/1628511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-methoxy-6-methyl-5-nitropyrimidineHCID 13080980—
ReactantHCID 178477797HCID 178477797—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Methoxy-4,6-dimethyl-5-nitropyrimidineHCID 6873730393.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

Methylzinc chloride (2.0 M solution in tetrahydrofuran, 14.8 mL, 29.6 mmol) was added dropwise to a solution of 4-chloro-2-methoxy-6-methyl-5-nitropyrimidine (4.01 g, 19.7 mmol) and tetrakis(triphenyl phosphine)palladium (1.90 mmol) in tetrahydrofuran (60 mL), and the mixture was stirred at 50° C. for 50 minutes. The mixture 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 pale yellow solid (3.37 g, 18.4 mmol, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-2b625742042941e7bada9ce7bf46a03a
Source noteuspto-grants-2014_07