HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl trifluoroacetate → 1-Trifluoroacetyl-4-hydroxy-4-phenylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 4-Phenylpiperidin-4-ol | HCID 96387 | — |
| Product | 1-Trifluoroacetyl-4-hydroxy-4-phenylpiperidine | HCID 1446513 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 25 g of 4-hydroxy-4-phenylpiperidine and 50 ml of ethyl trifluoroacetate is refluxed overnight and evaporated. The residue is taken up in benzene, the solution washed with 1N hydrochloric acid, dried and evaporated. The residue is recrystallized from ethyl acetate-petroleum ether, to yield the 1-trifluoroacetyl-4-hydroxy-4-phenylpiperidine melting at 123°-125°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04129655 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-85b342c49efc47bd97c2025dfa1e28f5 |
| Source note | uspto-grants-1978_12 |