HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → ethyl N-(1-benzylpiperidin-4-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | ethyl N-(1-benzylpiperidin-4-yl)carbamate | HCID 12641845 | 62.1% |
Reaction Steps
Ethyl chloroformate (30 g, 0.276 mol) was added at 0° C. to 4-amino-1-phenylmethylpiperidine (50 g, 0.262 mol) in pyridine (600 mL). After the addition, the mixture was kept at room temperature overnight, and the pyridine was then evaporated. The residue was extracted with methylene chloride; and the resulting solution washed with water, dried over sodium sulfate, and the methylene chloride evaporated to dryness. The residue was dissolved in diisopropyl ether. A white product precipitated, which was isolated by filtration to yield 42.71 g (62%) of ethyl (1-phenylmethyl-4-piperidyl)-carbamate, m.p. 100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05082847 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-0fe390e75e8e454c8ded6931d2c958fc |
| Source note | uspto-grants-1992_01 |