HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (1-Benzyl-4-piperidyl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-benzylpiperidine-4-carboxamide | HCID 3868064 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | (1-Benzyl-4-piperidyl)methanamine | HCID 1514444 | — |
Reaction Steps
To a solution of N-benzylisonipecotamide (7.34 g, 34 mmol) in 60 mL of anhydrous THF, was added, LiAlH4 (1.9 g, 51 mmol) and the mixture was stirred at room temperature for 10 minutes followed by heating to reflux for 3 h. The reaction was quenched by addition of 100 mL sat'd. sodium potassium tartrate, and was extracted with EtOAc (3×50 mL). The combined extracts were washed with 20 mL water and 20 mL brine then dried over MgSO4, filtered and concentrated to give the desired product. 1H-NMR (400 MHz, CDCl3) δ 7-13 (m, 5H), 3.42 (s, 2H), 2.91 (m, 2H), 2.59 (m, 2H), 1.97 (m, 2H), 1.62 (m, 2H), 2.21 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07608618B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-42a4dd0e0fa347d68a38ecc94efd04ac |
| Source note | uspto-grants-2009_10 |