HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamide → 4-(4-Bromo-3,5-dimethoxyphenyl)oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Bromo-1-(4-bromo-3,5-dimethoxyphenyl)ethanone | HCID 58432002 | — |
| Product | 4-(4-Bromo-3,5-dimethoxyphenyl)oxazole | HCID 58432125 | 58% |
Reaction Steps
A solution of 2-bromo-1-(4-bromo-3,5-dimethoxyphenyl)ethanone (0.8 g, 0.96 mmol) in formamide (7 mL) in an oven-dried flask under argon was heated at 100° C. for 10 hours then 110° C. for 5 hours. After cooling to room temp, EtOAc and saturated aqueous NaHCO3 were carefully added and the mixture was stirred for 15 minutes. It was then extracted with EtOAc twice and the combined organics were washed with H2O and brine, dried over Na2SO4 and concentrated. Purification by chromatography (20-40% EtOAc-hexanes) provided 4-(4-bromo-3,5-dimethoxyphenyl)oxazole as a yellow solid (0.387 g, 58% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09102643B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-002b3e726f744cac9655081b525b41ef |
| Source note | uspto-grants-2015_08 |