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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754683Generated: November 1, 2026

Boron tribromide → 1H-Pyrrolo[2,3-b]pyridin-5-ol

https://huagongshe.com/reaction/1754683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant5-methoxy-1H-pyrrolo[2,3-b]pyridineHCID 10307871—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1H-Pyrrolo[2,3-b]pyridin-5-olHCID 2203072244.7%

Reaction Steps

To a solution of 5-methoxy-1H-pyrrolo[2,3-b]pyridine (81, 0.5 g, 3 mmol) in tetrahydrofuran (20 mL) was added boron tribromide (1.5 g, 6.0 mmol) at 0° C. The reaction mixture was allowed to warm to room temperature, then stirred at room temperature for 3 hours. The reaction mixture was quenched by methanol. After repeated addition of methanol and removal of solvent, the concentrated reaction mixture was dissolved in ethyl acetate and water. The organic layer was collected, washed with brine, and dried over magnesium sulfate. After removal of solvent, the residue was purified by silica gel column chromatography eluting with ethyl acetate in hexane to provide the compound as an off-white solid (82, 0.18 g, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169250B2
Source datasetuspto-grants-2015_10
ORD IDord-36df65d0a04145b9b8d6b7a9fb7a5221
Source noteuspto-grants-2015_10