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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756346Generated: November 1, 2026

Acetone → 5-[(6-Bromo-2-pyridyl)-methyl]-tetrahydrofuran-2-one

https://huagongshe.com/reaction/1756346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium borohydrideHCID 4311764—
Reactant5-(6-Bromo-2-pyridyl)-4-oxo-pentanoic acid methyl esterHCID 15661799—
SolventMethanolHCID 887—
Product5-[(6-Bromo-2-pyridyl)-methyl]-tetrahydrofuran-2-oneHCID 1996649196%

Reaction Conditions

Temperature1.5 °C

Reaction Steps

A solution of 490 mg of 5-(6-bromo-2-pyridyl)-4-oxo-pentanoic acid methyl ester in 20 ml of methanol is mixed under ice cooling with 72 mg of sodium borohydride and stirred for 1 hour at 0-3° C. Then, 2 ml of acetone is added, stirred for 1 more hour and the reaction mixture is evaporated to dryness. The residue is distributed between water and ethyl acetate, the organic phase is dried on sodium sulfate and concentrated by evaporation. 421 mg of 5-[(6-bromo-2-pyridyl)-methyl]-tetrahydrofuran-2-one is obtained as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05440044
Source datasetuspto-grants-1995_08
ORD IDord-9ebf860b826341cd9a1c7c947556ae6d
Source noteuspto-grants-1995_08