Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15445561 | HCID 15445561 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 139004-92-5 | HCID 15667836 | 89% |
Reaction Steps
To a solution of 230 mL (0.23 mmol) of 1M lithium aluminum hydride in THF was added over 20 min a solution of (S)-N-benzylpiperidine-2-carboxamide in 150 mL of THF. The mixture was refluxed for 5 h, diluted with 500 ml of THF, cooled to -78° C. and quenched with a solution of 48 mL 1N aqueous sodium hydroxide in 200 mL THF. The resulting slurry was filtered through a Celite® pad and concentrated at reduced pressure to yield (S)-N-benzyl-2-aminomethylpiperidine (10.9 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05189046 |
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| Source dataset | uspto-grants-1993_02 |
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| ORD ID | ord-6c240e21cfbc43ad84c1742f8ba70bbc |
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| Source note | uspto-grants-1993_02 |
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