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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-(2-Fluorophenoxy)-2-(4-methoxy-3,5-dimethylphenyl)oxazolo[4,5-c]pyridine | HCID 71186536 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[6-(2-Fluorophenoxy)oxazolo[4,5-c]pyridin-2-yl]-2,6-dimethylphenol | HCID 136413239 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08907093B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-b2ce144e71494aa0a032b19947bb3658 |
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| Source note | uspto-grants-2014_12 |
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