Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382669Generated: November 1, 2026

Water → 4,4-Dimethyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/2382669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant4,4-Dimethyl-3,4-dihydroquinolin-2(1H)-oneHCID 14209945—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product4,4-Dimethyl-1,2,3,4-tetrahydroquinolineHCID 1321944187%

Reaction Conditions

Temperature50 °C

Reaction Steps

To 4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (7.6 g, 43 mmol) in THF (100 mL), was added lithium aluminum hydride (5 g, 134 mmole) portion wise with ice bath. The reaction mixture was warmed to 50° C. and stirred overnight. The reaction mixture was cooled to rt and treated with water (5 mL), 10% sodium hydroxide aqueous solution (5 mL) and water (15 mL). The resulting mixture was stirred for another 10 minutes. The mixture was filtered through Celite and the Celite was washed with ethyl acetate to a volume of approximately 50 mL. The resulting ethyl acetate solution was washed with brine (50 mL×2) and dried over MgSO4. Concentration of the filtrate and purification by silica gel column chromatography eluting with hexane/ethyl acetate (9/1) yielded 4,4-dimethyl-1,2,3,4-tetrahydro-quinoline 2-1 as a brown oil (6.0 g, 87% yield). MS: 162.0 (M+H)+; tR=1.47 min (method 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263588B2
Source datasetuspto-grants-2012_09
ORD IDord-028023d919f54554b9271d4bdea67b55
Source noteuspto-grants-2012_09