HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Benzyl 4-Hydroxy-1-piperidinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 4-Hydroxy-1-piperidinecarboxylate | HCID 2794620 | — |
Reaction Steps
69.1 ml of triethylamine and 70.2 ml of benzyl chloroformate are added in succession at 0° C. to a solution of 50 g of 4-hydroxypiperidine in 500 ml of dichloromethane. The resulting suspension is stirred at room temperature overnight and subsequently filtered. The residue which separates after concentration of the filtrate is taken up in ethyl acetate, washed with water and 1N hydrochloric acid, dried and concentrated. There are obtained 73.6 g of N-benzyloxycarbonyl-4-hydroxy-piperidine, Rf =0.56 (ethyl acetate/methanol 9:1), MS (EI): 235 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05545658 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-cc266aa4accb43aa97cb139f7ea5def3 |
| Source note | uspto-grants-1996_08 |