Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrocarbostyril | HCID 64796 | — |
| Reactant | Hexane, 2,5-dichloro-2,5-dimethyl- | HCID 80360 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18615010 | HCID 18615010 | 99% |
Reaction Steps
To a solution of 6,6,9,9-tetramethyl-3,4,6,7-hexahydro-1H-benzo[g]quinolin-2-one (1.0 g, 3.9 mmol, prepared by Friedel-Crafts alkylation/annulation of 2-oxo-1,2,3,4-tetrahydroquinoline with 2,5-dichloro-2,5-dimethylhexane in the presence of aluminum trichloride at ambient temperature in dichloromethane) in THF (10 mL) at ambient temperature was added LiAlH4 (11.7 mmol). The reaction mixture was heated to 80° C. and allowed to stir for 30 minutes. The reaction mixture was poured into aqueous saturated sodium potassium tartrate (100 mL), extracted with EtOAc (100 mL), dried (MgSO4), and concentrated to give 6,6,9,9-tetramethyl-1,2,3,4,6,7,8,9-octahydrobenzo[g]quinoline 978 mg (99%): 1H NMR (400 MHz, CDCl3) δ 6.88(s, 1H ArH), 6.41(s, 1H, ArH), 3.26(t, 2H, J=6.2 Hz, ring CH2), 2.71(t, 2H, J=4.0 Hz, ring CH2), 1.92(m, 2H, ring CH2), 1.63(s, 4H, 2CH2), 1.23(s, 12H, 4CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06545049B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-9c4c80bd3bee427c80997c63dfe2d414 |
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| Source note | uspto-grants-2003_04 |
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