HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63075Generated: October 26, 2026
6-Methoxy-alpha-tetralone → 1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol
https://huagongshe.com/reaction/63075
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Methoxy-alpha-tetralone | HCID 14112 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 13197589 | 68.4% |
Reaction Steps
TMS-cyanide (8.52 mL, 68.1 mmol) was added to a solution of 6-methoxy-1-tetralone (6.0 g, 34 mmol) in toluene (50 mL). A trace amount (˜20 mg) of zinc iodide was added, and the reaction was stirred at 60° C. for 16 hours. The solution was cooled to rt and diluted with THF (30 mL). This was added to a mixture of lithium aluminum hydride (2.58 g) in THF (50 mL), and the reaction mixture was heated at 42° C. for 2 h. The reaction was cooled to rt. EtOAc (10 mL) was slowly added, and the reaction stirred 30 min. Water (2 mL) and then 5N NaOH (1 mL) were slowly added, and the reaction stirred 1 h. The reaction mixture was diluted with EtOAc (100 mL), dried (MgSO4), and filtered through Celite. Purification by silica gel chromatography (10-20% MeOH/DCM) gave 4.82 g of 1-(aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447045B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-060b901605a7488ead9bd01c7620fa71 |
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| Source note | uspto-grants-2016_09 |
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