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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265254Generated: October 30, 2026

Hydrocarbostyril → HCID 18615010, compound

https://huagongshe.com/reaction/1265254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrocarbostyrilHCID 64796—
ReactantHexane, 2,5-dichloro-2,5-dimethyl-HCID 80360—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18615010HCID 1861501099%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545049B1
Source datasetuspto-grants-2003_04
ORD IDord-9c4c80bd3bee427c80997c63dfe2d414
Source noteuspto-grants-2003_04