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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956412Generated: October 25, 2026

Ethyl Bromide → 3-Ethoxy-2-methylpyridine

https://huagongshe.com/reaction/1956412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
Reactant2-Methylpyridin-3-olHCID 70719—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
Product3-Ethoxy-2-methylpyridineHCID 12875015—

Reaction Steps

Sodium metal (46.2 g) was dissolved in absolute ethanol (1 l) with stirring under nitrogen. 3-Hydroxy-2-methylpyridine (200 g prepared as described in C.A. 48, P4597 h) was added. The mixture was stirred at ambient temperature for 30 minutes and then a solution of bromoethane (150 ml) in absolute ethanol (100 ml) was added. The mixture was boiled under reflux for 5 hours then cooled and filtered. The filtrate was evaporated and the residue partitioned between dichloromethane and water. The organic layer was separated off and the aqueous layer extracted with dichloromethane. The combined organic extracts were dried and evaporated. The residue was distilled to give 3-ethoxy-2-methyl-pyridine b.p. 80°-84° C. (20 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780482
Source datasetuspto-grants-1998_07
ORD IDord-c05ac5b4791440ab8ecb0fd3523bb3b1
Source noteuspto-grants-1998_07