HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(1-(3-bromophenyl)-3-oxobutan-2-ylamino)-2-oxoacetate → Ethyl 4-(3-bromobenzyl)-5-methyloxazole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(1-(3-bromophenyl)-3-oxobutan-2-ylamino)-2-oxoacetate | HCID 86711487 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | Ethyl 4-(3-bromobenzyl)-5-methyloxazole-2-carboxylate | HCID 86711486 | 53.2% |
Reaction Steps
The solution of ethyl 2-(1-(3-bromophenyl)-3-oxobutan-2-ylamino)-2-oxoacetate (1.0 g, 2.9 mmol) in POCl3 (10 mL) was refluxed overnight. The mixture was concentrated, treated with H2O (40 mL), neutralized with aqueous NaHCO3 and extracted with EtOAc (3×20 mL). The combined organic layers were washed with H2O (20 mL), dried over Na2SO4, filtered, and concentrated to afford the crude product, which was purified by silica gel column chromatography (EtOAc:Petroleum ether=1:5) to afford ethyl 4-(3-bromobenzyl)-5-methyloxazole-2-carboxylate as a yellow oil (0.5 g, 51%). MS (ES+) C14H14BrNO3 requires: 323, 325 found: 324 [M+H]+, 326 [M+2+H]+(1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115120B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-2f8a815031a948ea8d8907c67b28b218 |
| Source note | uspto-grants-2015_08 |