HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl 5-(3,4-dimethoxy-5-nitrophenyl)-4-oxazolecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl isocyanoacetate | HCID 533707 | — |
| Reactant | 3,4-Dimethoxy-5-nitrobenzoyl chloride | HCID 21928615 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 5-(3,4-dimethoxy-5-nitrophenyl)-4-oxazolecarboxylate | HCID 21459162 | — |
Reaction Steps
A solution of 2.5 g of 3,4-dimethoxy-5-nitrobenzoyl chloride in 10 ml of absolute tetrahydrofuran is treated with 1.1 ml of ethyl isocyanoacetate and subsequently with a solution of 3.0 ml of triethylamine in 10 ml of tetrahydrofuran and stirred at room temperature for 48 hours. After distillation of the solvent, the residue is extracted with ethyl acetate/water. The crude product obtained after evaporation is chromatographed on a 20-fold amount of silica gel with ethyl acetate. After recrystallization from ethyl acetate/hexane there is obtained ethyl 5-(3,4-dimethoxy-5-nitrophenyl)-4-oxazolecarboxylate in the form of yellow crystals of m.p. 109°-110°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05633371 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-eb6ade9b578e419f95798fbe9a0df127 |
| Source note | uspto-grants-1997_05 |