HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → 1-[(4-Methylphenyl)methyl]piperidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-(4-Methylbenzyl)piperidin-4-one | HCID 11959541 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[(4-Methylphenyl)methyl]piperidin-4-amine | HCID 12641836 | 48.9% |
Reaction Steps
To 4.25 g (21 mmol) of 1-(4-methylbenzyl)-4-piperidinone 124 in 200 mL of anhydrous methanol was added 32.2 g (420 mmol) of ammonium acetate and 25 g of 3A molecular sieves. After stirring 30 min, 5.25 g (84 mmol) of sodium cyanoborohydride was added portionwise. After stirring 16 hours, the mixture was gravity filtered and the methanol evaporated under vacuum. The residue was partitioned between ether and ice/HCl. The acidic aqueous layer was extracted twice with ether, made basic with 50% aqueous NaOH and ice, and extracted with CH2Cl2 to give 2.1 g (48%) of the title amine 125 as a thick oil. GC/MS showed a molecular ion of 204. The product was used as is without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06521622B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-5f661590bdc4477988b338af869038e5 |
| Source note | uspto-grants-2003_02 |