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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401112Generated: October 30, 2026

Boron tribromide → 4-[6-(2-Fluorophenoxy)oxazolo[4,5-c]pyridin-2-yl]-2,6-dimethylphenol

https://huagongshe.com/reaction/1401112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
Reactant6-(2-Fluorophenoxy)-2-(4-methoxy-3,5-dimethylphenyl)oxazolo[4,5-c]pyridineHCID 71186536—
SolventDichloromethaneHCID 6344—
Product4-[6-(2-Fluorophenoxy)oxazolo[4,5-c]pyridin-2-yl]-2,6-dimethylphenolHCID 136413239—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 60 mg of 6-(2-fluorophenoxy)-2-(4-methoxy-3,5-dimethylphenyl)oxazolo[4,5-c]pyridine in 2 ml of dichloromethane was cooled to 0° C., and 0.4 ml of a 1 M solution of boron tribromide in dichloromethane were added over a period of 10 min. The mixture was stirred at 0° C. for 1 h and a further 0.2 ml of a 1 M solution of boron tribromide in dichloromethane was then added. The reaction was then stirred at room temperature for 16 h. For work-up, saturated aqueous sodium bicarbonate solution was added slowly to the reaction mixture. The precipitate was filtered off, washed with water and dried under reduced pressure. This gave 41 mg (71%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907093B2
Source datasetuspto-grants-2014_12
ORD IDord-b2ce144e71494aa0a032b19947bb3658
Source noteuspto-grants-2014_12