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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973672Generated: October 31, 2026

3-Amino-5,5-dimethyl-2-cyclohexen-1-one → 5,6,7,8-Tetrahydro-3,7,7-trimethylquinoline-5-one

https://huagongshe.com/reaction/1973672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-5,5-dimethyl-2-cyclohexen-1-oneHCID 136680—
Reactant3-Ethoxy-2-methyl-2-propenalHCID 559198—
Product5,6,7,8-Tetrahydro-3,7,7-trimethylquinoline-5-oneHCID 417519260.8%

Reaction Steps

A mixture of 3-amino-5,5-dimethylcyclohex-2-enone (27.8g., 0.2 mol.) and 2-methyl-3-ethoxyacrolein (22.8 g., 0.2 mol.), in an apparatus equipped for downward distillation, was heated in an oil bath at 120° until the theoretical quantity of distillate was collected (13 ml.) The cooled residue was diluted with 2N HCl (50 ml.), extracted with ethyl acetate (3 × 50 ml.) and the combined extracts discarded. The aqueous solution was adjusted to pH 9.0 with sodium carbonate and extracted with ethyl acetate (3 × 50 ml.). The combined extracts were dried (MgSO4) and the solvent removed in vacuo and the residual oil distilled to give the title compound as a colourless oil (23 g., 53%) b.p. 83°/0.2 mm Hg. (RT = 2 min., 2% OV17, T=150° C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998831
Source datasetuspto-grants-1976_12
ORD IDord-3cc924f443b945d093a5403c0c48221f
Source noteuspto-grants-1976_12