HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Acetate → Ethyl 2-(1-benzyloxycarbonyl-3-azetidinyl)acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Ethyl hydrogen (1-benzyloxycarbonyl-3-azetidinyl)malonate | HCID 53765389 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 2-(1-benzyloxycarbonyl-3-azetidinyl)acrylate | HCID 54322358 | 86.3% |
Reaction Steps
To 732 mg (2.28 mmol) of ethyl hydrogen (1-benzyloxycarbonyl-3-azetidinyl)malonate dissolved in 70 ml of acetonitrile were added 1.05 g (5.67 mmol) of Eshenmoser's salt and a catalytically effective amount of potassium acetate, followed by 4.5 hours of heating under reflux. After evaporation of the solvent, the resulting residue was mixed with 100 ml of ethyl acetate, washed with 10% citric acid aqueous solution, 10% sodium sulfite aqueous solution and saturated brine in that order, and then dried over anhydrous sodium sulfate. By evaporating the solvent, 569 mg (86%) of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849757 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-811ea7ee01dd4281abbeeec749354545 |
| Source note | uspto-grants-1998_12 |