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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450179Generated: October 25, 2026

2-Chloro-5-nitropyrimidine → 2-Methoxy-5-nitropyrimidine

https://huagongshe.com/reaction/450179

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitropyrimidineHCID 82544—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product2-Methoxy-5-nitropyrimidineHCID 352900134.3%

Reaction Steps

To a solution of sodium methoxide (0.090 g of sodium) in MeOH (12 mL) was added 0.486 g (3.03 mmol) of 2-chloro-5-nitropyrimidine, and the mixture was heated under reflux for 1 hr. After cooling, the mixture was concentrated in vacuo, extracted with EtOAc, and washed with water. The aqueous layer was extracted with CHCl3 and the combined organic layers were dried (Na2SO4), and concentrated, to give 0.347 g (75% yield) of 2-methoxy-5-nitropyrimidine as a yellow powder: 1H NMR (CDCl3) δ9.31 (s, 2H), 4.17 (s, 3H); LCMS (APCI+) m/z: 156 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486939B2
Source datasetuspto-grants-2013_07
ORD IDord-160f4f9dca0f416a938b965dced57a0a
Source noteuspto-grants-2013_07