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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727795Generated: October 29, 2026

1,3-Cyclohexanedione → 3-(1,2,3,4-Tetrahydro-1-quinolinyl)-2-cyclohexen-1-one

https://huagongshe.com/reaction/727795

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-CyclohexanedioneHCID 10434—
Reactant1,2,3,4-TetrahydroquinolineHCID 69460—
Product3-(1,2,3,4-Tetrahydro-1-quinolinyl)-2-cyclohexen-1-oneHCID 1982508915.6%

Reaction Steps

A mixture of 1,2,3,4-tetrahydroquinoline (5 g) and 1,3-cyclohexanedione (4.21 g) was heated at ca. 150° for 5 h. The cooled reaction mixture was purified by FCC eluting with ethyl acetate to give the title compound (1.33 g) as an oil, t.l.c. (ethyl acetate) Rf 0.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045545
Source datasetuspto-grants-1991_09
ORD IDord-1460907208b4404892012a734759fd70
Source noteuspto-grants-1991_09