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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859393Generated: November 2, 2026

Tetrahydrofuran → 1-(6-Chloropyridin-2-yl)ethanone

https://huagongshe.com/reaction/1859393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant6-Chloropyridine-2-carbonitrileHCID 118424—
ReactantHCID 178418373HCID 178418373—
SolventDiethyl EtherHCID 3283—
Product1-(6-Chloropyridin-2-yl)ethanoneHCID 11579167—

Reaction Steps

A solution of 2-chloro-6-cyanopyridine (50 g) in THF (400 ml) is cooled to −5° C. and a solution of methylmagnesium iodide in diethyl ether (3 M, 200 ml) is added. After 1 h at 0° C. the ether is destilled off and the THF-mixture is heated to 60° C. for 1 h. The THF is evaporated and the residue is treated with ice water and acidified with 2 M hydrochloric acid. The water phase is extracted with dichloromethane and after drying and evaporation of the organic phase, the residue is purified by silica-gel flash chromatography. The title compound is obtained as an oil (11.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528456B2
Source datasetuspto-grants-2003_03
ORD IDord-e9a636cca3c340d69cd851d12531c500
Source noteuspto-grants-2003_03