HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Benzyl 3-methyl-4-oxopiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Methylpiperidin-4-one hydrobromide | HCID 20094587 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl 3-methyl-4-oxopiperidine-1-carboxylate | HCID 15233096 | — |
Reaction Steps
To a mechanically stirred mixture of benzylchloroformate (33.1 mL, 232 mmol, 105 mol %), sodium bicarbonate (37.2 g, 442 mmol, 200 mol %), ether (250 mL), and water (250 mL) is added 3-methyl-4-piperidone hydrobromide salt (42.9 g, 221 mmol) in portions over 10 min. The resultant mixture is stirred for 2 h and the organic phase separated. The aqueous phase is extracted with ether (2×150 mL) and the combined organics dried (MgSO4), filtered, and concentrated to an oily residue. This residue crystallized on standing at 23° C. and was recrystallized from hexanes/ethyl acetate to give N-benzyloxycarbonyl-3-methyl-4-piperidone as a solid: 51.2 g; 93%; mp 33°-35° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130321 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-b217e9c4e5ec4ac482ce11b78b7296c4 |
| Source note | uspto-grants-1992_07 |