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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840872Generated: October 30, 2026

Hydrochloric Acid → 6-Acetyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1840872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant6-bromo-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-oneHCID 10729589—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product6-Acetyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-oneHCID 2344470267%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 6-bromo-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (Intermediate 4, 270 mg, 1.06 mmol) in 5 ml of THF was first degassed by bubbling with argon for 30 min. Tributyl(1-ethoxyvinyl)tin (766 mg, 2.12 mmol) and PdCl2(PPh3)2 (37mg, 0.05 mmol) were added. After stirring at 80° C. for 18 h, the mixture was cooled to room temperature and 3 mL of 10% HCl was added. The mixture was then stirred for another 30 min before extracted with ethyl acetate (3×10 mL). The combined organic layer was washed with brine (1×10 mL), dried (MgSO4) and concentrated at reduced pressure. Purification by flash chormatography (50:50 hexane/ethyl acetate) yielded the title compound as a white solid (154 mg, 67% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683092B1
Source datasetuspto-grants-2004_01
ORD IDord-2284227a08b34a7f97e9de14f83ae5b1
Source noteuspto-grants-2004_01