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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233729Generated: October 25, 2026

Water → 2-(6-Chloro-2-methoxypyridin-3-yl)ethan-1-ol

https://huagongshe.com/reaction/233729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthylene OxideHCID 6354—
Reactant2-Chloro-6-methoxypyridineHCID 87009—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-(6-Chloro-2-methoxypyridin-3-yl)ethan-1-olHCID 19703680—

Reaction Steps

To a solution of 1.0 g (7.0 mmol) of 2-chloro-6-methoxypyridine in 20 ml of dry THF cooled to -78° C. was added 10.9 ml (1.6M in hexanes, 17.4 mmol) n-BuLi under an atmosphere of nitrogen. The temperature of the mixture was allowed to raise to -40° C. before an addition of 4 ml ethylene oxide in 6 ml ether. The mixture was warmed to room temperature, 50 ml water was added and the aqueous layer was separated and extracted with 2×100 ml EtOAc. The organic extracts were combined, washed once with water, dried with Na2SO4, and concentrated in vacuo. The crude material was purified by dry column flash chromatography (hexane/EtOAc) to afford 0.22 g of 3-(2-hydroxyethyl)-6-chloro-2-methoxypyridine as a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05593993
Source datasetuspto-grants-1997_01
ORD IDord-825c65e13c79422983a8fc57b77d283f
Source noteuspto-grants-1997_01