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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707613Generated: October 29, 2026

2-Butenamide, N-(4-bromophenyl)-3-methyl- → 6-bromo-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1707613

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butenamide, N-(4-bromophenyl)-3-methyl-HCID 532095—
ReactantAluminum(III) ChlorideHCID 6451240—
Product6-bromo-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-oneHCID 10729589—

Reaction Conditions

Temperature130 °C

Reaction Steps

To 6.7 g (26.02 mmol) of molten N-(4-bromophenyl)3,3-dimethylacrylamide (heated to 135° C.) was added 4.15 g (31.09) of aluminum chloride over 25 minutes. The reaction mixture was stirred at 130° C. for 16 hours and then treated with a further 1 g of aluminum chloride. The reaction mixture was heated at 130° C. for a further 9 hours and then cooled to room temperature. The reaction was then quenched by the slow addition of 100 ml of ice cold water with slight warming of flask to facilitate mixing. The mixture was extracted with 1×100 ml and 4×50 ml of ether. The organic extracts were combined and washed with 25 ml of saturated NaCl solution and then dried (MgSO4). The solvent was removed in vacuo and the residue purified by flash chromatography (silica; 30% ethyl acetate in hexanes) to give the title compound as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354752
Source datasetuspto-grants-1994_10
ORD IDord-020457bb2e934523b5acf665fdce07dd
Source noteuspto-grants-1994_10