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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703942Generated: October 31, 2026

Gamma-Butyrolactone → 4-Hydroxy-1-(3-pyridyl)-1-butanone

https://huagongshe.com/reaction/703942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGamma-ButyrolactoneHCID 7302—
Reactant3-BromopyridineHCID 12286—
ReactantHCID 178418244HCID 178418244—
SolventDiethyl EtherHCID 3283—
Product4-Hydroxy-1-(3-pyridyl)-1-butanoneHCID 10781977%

Reaction Steps

A solution of 10.0 g (63.3 mmol) of 3-bromopyridine in 100 ml of ether was cooled to -78° C., to which 40 ml (64 mmol) of 1.6 M n-butyllithium hexane solution was added dropwise with stirring. After completion of the addition, the mixture was stirred for further 15 minutes, to which the solution of 5.45 g (63.3 mmol) of γ-butyrolactone in 15 ml of ether was added dropwise, and stirred for further 1 hour at -78° C.-room temperature. To the reaction mixture an aqueous solution of ammonium chloride, and the resultant substance was extracted with ethyl acetate. The extract was washed with water and dried, and the solvent was evaporated off. The residue was purified with silica gel column chromatography (CHCl3 -MeOH (9:1)) and recrystallized from ethyl acetate-isopropyl ether, to give 8.0 g (77%) of 4-(3-pyridyl)-4-oxobutanol. m.p. 36°-37° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985447
Source datasetuspto-grants-1991_01
ORD IDord-ca50447f2e67423383dce2980d586790
Source noteuspto-grants-1991_01