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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723677Generated: November 1, 2026

4,6-Dichloro-5-nitropyrimidine → 4-chloro-6-methoxy-5-nitropyrimidine

https://huagongshe.com/reaction/1723677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-5-nitropyrimidineHCID 20312—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product4-chloro-6-methoxy-5-nitropyrimidineHCID 25220474%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium methoxide (2.70 g, 50.0 mmol) was added portionwise over 10 min to a 0° C. suspension of 4,6-dichloro-5-nitropyrimidine (4.85 g, 25.0 mmol) in methanol (90 ml). On complete addition the mixture was stirred at 0° C for 2 h. The precipitate was filtered and the filtrate evaporated. The residue was suspended in isohexane and filtered. The filtrate was evaporated and the residue purified by flash column chromatography on silica, eluting with 5% ethyl acetate in isohexane. Collecting appropriate fractions gave 4-chloro-6-methoxy-5-nitropyrimidine (3.50 g, 74%) as a white solid: δH (400 MHz, CDCl3) 4.15 (3H, s), 8.65 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485640B2
Source datasetuspto-grants-2009_02
ORD IDord-07e7aec29ab64322bb7090cab3ebf0c3
Source noteuspto-grants-2009_02