HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-Benzyl-4-(phenylamino)piperidine-4-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 19935652 | HCID 19935652 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Benzyl-4-(phenylamino)piperidine-4-methanol | HCID 3017230 | 76% |
Reaction Steps
Sodium borohydride (2 g) was added portionwise to a stirred solution of 4-(N-phenylamino)-1-phenylmethyl-piperidine-4-carboxaldehyde (2 g) in methanol at room temperature. After stirring at room temperature for 2 hours the mixture was diluted with water, extracted with chloroform and the combined extracts washed and dried. After removal of the solvent, the crude product was purified by chromatography on silica gel, using chloroform/methanol (38:1) as eluant, to give the title compound (1.53 g) 4-(N-phenylamino)--1-phenylmethyl-4-piperidinylmethanol is then converted to sufentanil following the method described in U.S. Pat. No. 4,179,469 and as illustrated by FIG. 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420280 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-3f041f1a149f4c3da5afef44e7d0f088 |
| Source note | uspto-grants-1995_05 |