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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453631Generated: October 30, 2026

1-Iodoheptane → 6-Acetyl-1-heptyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1453631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodoheptaneHCID 20274—
ReactantSodium hydrideHCID 24758—
Reactant6-Acetyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-oneHCID 23444702—
SolventDimethylformamideHCID 6228—
Product6-Acetyl-1-heptyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-oneHCID 2344469966%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (21.0 mg, 90.0 mmol) was slowly added into a solution of 6-acetyl-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (Compound 28, 98.0 mg, 45.0 mmol) in 3 mL of DMF at 0° C. After stirring at 0° C. for 10 min, 1-iodoheptane (30.5 mg, 135.0 mmol) was added to the reaction mixture and the ice-bath was removed. The reaction mixture was allowed to stir for 2 h and then quenched with ice water. The resulting solution was then extracted with ether (3×10 mL), washed with brine (1×10 mL), dried (MgSO4) and concentrated at reduced pressure. Purification by flash chromatography (75:25 hexane/ethyl acetate) yielded the title compound (93.6 mg, 66% yield) as a colorless oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476673B2
Source datasetuspto-grants-2009_01
ORD IDord-78c5cc729a4149928f1ee9ad359bca33
Source noteuspto-grants-2009_01