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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445613Generated: October 29, 2026

Methanol → 5-Bromo-2-methoxy-3-nitropyridine

https://huagongshe.com/reaction/445613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant5-Bromo-2-chloro-3-nitropyridineHCID 7019412—
Product5-Bromo-2-methoxy-3-nitropyridineHCID 15645664—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a vial are introduced 1 ml of MeOH and 50.8 mg (2.21 mmol) of Na. After dissolution of the metal, the solution was added to a suspension of 5-bromo-2-chloro-3-nitropyridine (Matrix, Columbia, USA, 500 mg, 2.11 mmol) in MeOH (2 ml). The reaction mixture is stirred for 1 h at 0° C. and for 15 h at rt, then concentrated and quenched with water. The precipitate was filtered, washed with water (2×) and dried under vacuum to give the title compound as a pale yellow solid (HPLC: tR 3.06 min (Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476294B2
Source datasetuspto-grants-2013_07
ORD IDord-1113385c49654c25adaa1c1eb841d0e4
Source noteuspto-grants-2013_07