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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011331Generated: November 1, 2026

Acetic Acid → furo(3,4-b)pyridin-5(7H)-one

https://huagongshe.com/reaction/1011331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFuro[3,4-b]pyridine-5,7-dioneHCID 69688—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Productfuro(3,4-b)pyridin-5(7H)-oneHCID 81943927%

Reaction Conditions

Temperature15 °C

Reaction Steps

A solution of furo[3,4-b]pyridine-5,7-dione (3.0 g, 20 mmol) in THF (20 mL) is treated with sodium borohydride (0.75 g, 20 mmol). The reaction mixture is placed under an argon atmosphere and the temperature is maintained at 15° C. with a water bath. Acetic acid (2.4 g, 39 mmol) is added dropwise at 15° C. The reaction mixture is stirred for 4 h and is then concentrated on a rotary evaporator. The crude residue is then treated with acetic acid (8 mL.) and acetic anhydride (8.0 mL) and heated at 100° C. overnight. The reaction mixture is cooled and concentrated. The residue is purified by chromatography (silica gel, gradient elution 30% EtOAc/hexane to 50% EtOAc/hexane). The product containing fractions are concentrated to give the title compound as a white solid (360 mg, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977351B2
Source datasetuspto-grants-2011_07
ORD IDord-193fde5c08ed4a3eb35af5303ef872e8
Source noteuspto-grants-2011_07