HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 54435245, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14011078 | HCID 14011078 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54435245 | HCID 54435245 | — |
Reaction Steps
Sodium borohydride (1.13 g, 30 mmol) was added to a stirred suspension of 1-benzoyl-4-(4-acetamidobenzoyl)piperidine (10.0 g, 29 mmol) in ethanol (300 ml), cooled in a water bath. The mixture was stirred at room temperature for 1 hour then additional sodium borohydride (1.13 g, 30 mmol) was added and stirring was continued for 2 hours. The solvent was evaporated under reduced pressure and water (200 ml), HCl--H2O (6M, 15 ml) and methanol (15 ml) were added. The mixture was extracted with dichloromethane (4×200 ml) and the combined organic fractions were dried (Na2SO4) and evaporated under reduced pressure to give an off-white solid which was crystallized from ethanol to give the piperidine as white crystals. (5.77 g, 57%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112824 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-195f5f1dc36949b5b5b1a2b1ef93d8a8 |
| Source note | uspto-grants-1992_05 |