HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Tetralone → 1-(Aminomethyl)-1,2,3,4-tetrahydronaphthalen-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Tetralone | HCID 10724 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Aminomethyl)-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 12914859 | 73% |
Reaction Steps
Five and one-half g of trimethylsilylcyanide is added to a mixture of 7.3 g of 1-tetralone and 10 mg of zinc iodide. The mixture is stirred at room temperature overnight. It is dissolved in 25 ml dry THF and slowly added to a suspension of 2.3 g of lithium aluminumhydride in 40 ml of THF. Reaction is refluxed for three hours and upon cooling, carefully quenched with water. Precipitate is filtered and aqueous solution is diluted with 100 ml 1N NaOH. It was extracted with ether (3×100 ml), dried over anhydrous MgSO4, filtered, and ether evaporated yielding an oil which solidifies upon standing giving 6.4 g (73%) of (1-hydroxy-1,2,3,4-tetrahydronaphthyl)methylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04791103 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-329f329a0cdd4493b7078fea42a259cc |
| Source note | uspto-grants-1988_12 |