HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Aminomethyl-5-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Fluoride | HCID 5235 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 6-Methoxy-1-trimethylsilyloxy-tetralin-1-carbonitrile | HCID 187279 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 1-Aminomethyl-5-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 22462912 | — |
Reaction Steps
Under nitrogen, to the slurry of lithium aluminum hydride (11.4 g) in tetrahydrofuran (200 ml) was added 6-methoxy-1-(trimethylsilanyloxy)-1,2,3,4-tetrahydronaphthalene-1-carbonitrile (41.3 g) in tetrahydrofuran (200 ml) dropwise at 5° C., and the mixture was stirred at the same temperature for 1 hour and at room temperature for 2 hours. To the mixture were added sodium fluoride (12.6 g) and water (16.2 ml) at 5° C., and the mixture was vigorously stirred at room temperature for 30 minutes. The precipitate was removed by filtration and the filter cake was washed with ethyl acetate-ethanol (95:5). The filtrate was evaporated in vacuo to afford 1-aminomethyl-5-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol (28.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06391915B2 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-b5acc5f87e8d42a8979f7370ac77ff91 |
| Source note | uspto-grants-2002_05 |