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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598058Generated: November 2, 2026

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

https://huagongshe.com/reaction/598058

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-6-methyl-5-nitropyrimidineHCID 275294—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product2-Chloro-4-methoxy-6-methyl-5-nitropyrimidineHCID 1308097965.2%

Reaction Conditions

Temperature-10 °C

Reaction Steps

2,4-Dichloro-6-methyl-5-nitropyrimidine (3.0 g, 14.4 mmol) was dissolved in methanol (30 mL). The solution was cooled to −10° C. and sodium methoxide (25% in methanol, 3.3 mL, 14.4 mmol) was added drop wise. After 10 minutes, the solution was quenched with acetic acid (5 mL) and concentrated. The residue was suspended in saturated sodium bicarbonate and extracted twice with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and concentrated. Flash chromatography (5% ethyl acetate/hexanes) gave 1.91 g (65% yield) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897607B2
Source datasetuspto-grants-2011_03
ORD IDord-29520bfb21f447d98738019874294ace
Source noteuspto-grants-2011_03