HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N-(1-methyl-3-piperidinylmethyl)-N-cyclooctylmethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Methyl-3-cyclooctylmethylaminocarbonylpiperidine | HCID 20081674 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(1-methyl-3-piperidinylmethyl)-N-cyclooctylmethylamine | HCID 14747665 | 85.8% |
Reaction Steps
To 50 ml of distilled tetrahydrofuran were added 3.2 g of 1-methyl-3-cyclooctylmethylaminocarbonylpiperidine and 1.5 g of lithium aluminum hydride. The mixture was refluxed for 10 hours under a nitrogen current. After cooling, the reaction mixture was mixed with methanol and 2N sodium hydroxide. The resulting mixture was stirred and then the insoluble materials were removed by filtration. The filtrate was concentrated. The residue was distilled in a glass tube over under reduced pressure to obtain 2.6 g of N-(1-methyl-3-piperidinylmethyl)-N-cyclooctylmethylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05227381 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-5218164b65c84f2a9ffadfc53496820f |
| Source note | uspto-grants-1993_07 |