HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(Aminomethyl)-1,2,3,4-tetrahydronaphthalen-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Fluoride | HCID 5235 | — |
| Reactant | 1-Trimethylsilyloxy-1-cyano-1,2,3,4-tetrahydronaphthalene | HCID 11746907 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Aminomethyl)-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 12914859 | 97.4% |
Reaction Steps
Under nitrogen, to the suspension of lithium aluminum hydride (8.4 g) in tetrahydrofuran (120 ml) was dropwise added 1-trimethylsilyloxy-1-cyano-1,2,3,4-tetrahydro-naphthalene (27 g) in tetrahydrofuran (120 ml) at 5° C., and the mixture was stirred at room temperature for 24 hours. To the mixture were added sodium fluoride (37 g) and water (12 ml) at 5° C., and the mixture was vigorously stirred at room temperature for 30 minutes. The precipitate was removed by filtration. The filtrate was evaporated in vacuo to give 1-aminomethyl-1-hydroxy-1,2,3,4-tetrahydronaphthalene (19 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07217706B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-5a7ec57f0d484e49acc782760beb11bb |
| Source note | uspto-grants-2007_05 |