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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695756Generated: October 27, 2026

Ethanol → 5-Bromo-2-ethoxy-3-nitropyridine

https://huagongshe.com/reaction/1695756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodiumHCID 5360545—
Reactant5-Bromo-2-chloro-3-nitropyridineHCID 7019412—
Product5-Bromo-2-ethoxy-3-nitropyridineHCID 58255782—

Reaction Steps

Sodium (3.22 g) was dissolved in absolute ethanol (100 ml) and added dropwise to a suspension of 5-bromo-2-chloro-3-nitropyridine (30.2 g) in ethanol (100 ml) at 0° C. over 10 mins. The cold bath was removed and the reaction stirred at RT for 18 h. The reaction was evaporated to approximately half its volume then diluted with saturated ammonium chloride (aq) (600 ml). The reaction was stirred at RT overnight then the solids were filtered and rinsed well with water. The solids were dissolved in hot ethanol (100 ml) then diluted with hot water (500 ml) and stirred with cooling to RT for 2 hr. The solids were collected and rinsed well with water then suction dried and vacuum dried to give the title compound (26.4 g) as a dark brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163743B2
Source datasetuspto-grants-2012_04
ORD IDord-0e50e6c0e24f4fc4b02391c12120e01f
Source noteuspto-grants-2012_04