HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Ethyl 4-[(2,6-dichlorophenyl)amino]-1-piperidinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 4-[(2,6-dichlorophenyl)imino]-1-piperidinecarboxylate | HCID 23339072 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Ethyl 4-[(2,6-dichlorophenyl)amino]-1-piperidinecarboxylate | HCID 23338997 | — |
Reaction Steps
To a stirred and refluxing mixture of 250 parts of ethyl 4-[(2,6-dichlorophenyl)imino]-1-piperidinecarboxylate in 160 parts of methanol and 160 parts of 2-propanol are added portionwise 30 parts of sodium borohydride. Upon completion, stirring at reflux temperature is continued for one hour. The warm reaction mixture is poured onto water and the product is extracted with methylbenzene. The extract is dried and evaporated. The residue is crystallized from a mixture of 160 parts of 2,2'-oxybispropane and 160 parts of petroleumether, yielding 96 parts of ethyl 4-[(2,6-dichlorophenyl)-amino]-1-piperidinecarboxylate; mp. 107.2°-116.6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04126689 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-a8e6786ffce34fc3b682e6f65f2c9f27 |
| Source note | uspto-grants-1978_11 |