HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium hydroxide ethanol → Ethyl hydrogen (1-benzyloxycarbonyl-3-azetidinyl)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium hydroxide ethanol | HCID 21946426 | — |
| Reactant | Diethyl (1-benzyloxycarbonyl-3-azetidinyl)malonate | HCID 54152329 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl hydrogen (1-benzyloxycarbonyl-3-azetidinyl)malonate | HCID 53765389 | — |
Reaction Steps
To 13.43 g (38.33 mmol) of diethyl (1-benzyloxycarbonyl-3-azetidinyl)malonate dissolved in 130 ml of ethanol was added 38.44 ml of 1N potassium hydroxide ethanol solution, followed by overnight stirring at room temperature. After evaporation of the solvent, the resulting residue was mixed with 10% citric acid aqueous solution, extracted with chloroform (200 ml×3) and then dried over anhydrous sodium sulfate. By evaporating the solvent, quantitative amount 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-ab1491196a9c433e8b2f716691c23701 |
| Source note | uspto-grants-1998_12 |