HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-Piperidinemethanol, 4-(phenylamino)-1-(2-phenylethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(N-phenylamino)-1-(2-phenylethyl)piperidine-4-carboxaldehyde | HCID 19935659 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Piperidinemethanol, 4-(phenylamino)-1-(2-phenylethyl)- | HCID 12298204 | 82% |
Reaction Steps
Sodium borohydride (2 g) was added portionwise to a stirred solution of 4-(N-phenylamino)-1-(2-phenylethyl)piperidine-4-carboxaldehyde (2 g) in methanol (2 g) at room temperature for 2 hours. The mixture was diluted with water, extracted with chloroform and the combined extracts washed, dried over MgSO4 and concentrated. The residue was chromatographed on silica gel, using chloroform-methanol 19:1 as eluant, to afford 4-(N-phenylamino)-1-(2-phenylethyl)-4-piperidinylmethanol (1.65 g), m.p. 98°-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420280 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-35de2818d95847eebb2eea74c0f03d1e |
| Source note | uspto-grants-1995_05 |