HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 2-(4-Tert-butylthiazol-2-yl)-5-hydroxybenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 19092726 | HCID 19092726 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Tert-butylthiazol-2-yl)-5-hydroxybenzofuran | HCID 10858665 | 95.7% |
Reaction Steps
To a cooled solution of 4-tert-butyl-2-(5-methoxybenzofuran-2-yl)thiazole (1.0 g) in dichloromethane (10 ml), 1M solution of boron tribromide in dichloromethane (7 ml) was added dropwise at 5° C. After being stirred for 3 hours, the resulting solution was poured into a mixture of ice and aqueous sodium hydrogen carbonate. The resulting precipitates were collected by filtration and dissolved in a mixture of tetrahydrofuran and water. The solution was concentrated to give crystals of 4-tert-butyl-2-(5-hydroxybenzofuran-2-yl)thiazole (0.91 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05296495 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-046100f290044a53b67c82b0d0b67fd1 |
| Source note | uspto-grants-1994_03 |