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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591252Generated: October 31, 2026

Acrolein → 3-Chloro-7,8-dihydroquinolin-5(6H)-one

https://huagongshe.com/reaction/1591252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcroleinHCID 7847—
ReactantOxalyl chlorideHCID 65578—
Reactant2,3-Dichloro-2-propenalHCID 150516—
Reactant3-Aminocyclohexan-1-oneHCID 21873184—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-Chloro-7,8-dihydroquinolin-5(6H)-oneHCID 10997654—

Reaction Steps

In reaction 3 of Scheme 1, a solution of oxalyl chloride in methylene chloride is added dropwise to a solution of chloromalondialdehyde III in methyene chloride and a phase transfer catalyst, such as dimethylformamide, under inert reaction conditions. The reaction mixture is stirred at room temperature until conversion to the corresponding 2,3-dichloroacrolein is complete. In reaction 4 of Scheme 1, a solution of 1-amino-cyclohexan-3-one VI in dimethylformamide is added dropwise to the above acrolein to form the corresponding 3-chloro-5,6,7,8-tetrahydroquinolin-5-one VII. The reaction, generally carried out overnight, will be in the temperature range between about 60° C. to about 80° C., preferably about 70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206367
Source datasetuspto-grants-1993_04
ORD IDord-4de99e44c85c41d488652a206de3a760
Source noteuspto-grants-1993_04