HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 13094167, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13094166 | HCID 13094166 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13094167 | HCID 13094167 | 35% |
Reaction Steps
To a stirred mixture of 4.5 parts of ethyl 1-[4-cyano-4-(2-pyridinyl)-1-cyclohexenyl]-4-phenyl-4-piperidinecarboxylate and 80 parts of ethanol are added portionwise 0.4 parts of sodium borohydride. Upon completion, stirring is continued first overnight at room temperature and further for 30 minutes at reflux. The reaction mixture is cooled and poured onto water. The product is extracted with dichloromethane. The extract is dried, filtered and evaporated. The residue is crystallized from 2-propanol, yielding 2 parts (35%) of ethyl 1-[4-cyano-4-(2-pyridinyl)cyclohexyl]-4-phenyl-4-piperidinecarboxylate; mp. 157.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04369184 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-9bd39efd566e4ffdb12b28a532a07b97 |
| Source note | uspto-grants-1983_01 |