HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Tributylstannyl)furan → 7-(2-Furyl)-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| Reactant | 7-Bromo-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole | HCID 12148969 | — |
| Catalyst | HCID 178424406 | HCID 178424406 | — |
| Solvent | P-Xylene | HCID 7809 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 7-(2-Furyl)-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole | HCID 21907392 | 99% |
Reaction Steps
7-Bromo-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole (300 mg, 0.90 mmol) and dichlorobis(tri-o-tolylphosphine)palladium(II) (71 mg, 0.09 mmol) were dissolved in p-xylene (3 mL) and stirred for 10 min at room temperature under a nitrogen atmosphere. 2-(Tributylstannyl)furan (449 mg, 1.26 mmol) was added and the mixture was refluxed for 4 hours. The mixture was cooled to room temperature, diluted with a saturated solution of ammonium chloride and extracted with EtOAc. The organic extracts were washed with water, then brine and dried over MgSO4 and concentrated. Purification by flash chromatography (20%-30% EtOAc/petroleum ether) gave the title compound as a white solid (99% yield, m.p 120-121° C.); MS m/e 322 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794403B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-e9901114742246aeaec9e47ae8f6dd76 |
| Source note | uspto-grants-2004_09 |