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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977594Generated: October 29, 2026

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

https://huagongshe.com/reaction/977594

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 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 numberUS05614634
Source datasetuspto-grants-1997_03
ORD IDord-a7a8db29ac714ebdbd6221408e500677
Source noteuspto-grants-1997_03