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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557172Generated: October 25, 2026

Methanol → 7-Bromofuro[3,2-c]pyridin-4(5H)-one

https://huagongshe.com/reaction/557172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-bromobutanimideHCID 67184—
Reactant4H,5H-furo(3,2-c)pyridin-4-oneHCID 288746—
SolventAcetonitrileHCID 6342—
Product7-Bromofuro[3,2-c]pyridin-4(5H)-oneHCID 17985527—

Reaction Steps

Add N-bromosuccinimide (63.16 g, 354.9 mmol) as a solution in anhydrous acetonitrile (480 mL) to a suspension of 5H-furo[3,2-c]pyridin-4-one (36.9 g, 273 mmol) in anhydrous acetonitrile (740 mL) at 0° C. over 1 hour. Warm to room temperature, add anhydrous methyl alcohol (1.5 L) and stir at room temperature for 18 hours. Quench with water (20 ml) and saturated sodium bicarbonate (20 mL), concentrate to a volume of 1.3 liters, and pour into water (1.3 L). Collection of the precipitate by filtration and drying (vacuum oven 2 days 40-60° C.) gives the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058425B2
Source datasetuspto-grants-2011_11
ORD IDord-9bd1f2e713f14c15b1a56ea1de3a101f
Source noteuspto-grants-2011_11