HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973671Generated: October 31, 2026
Triethylamine → 5,6,7,8-Tetrahydro-3,7,7-trimethylquinoline-5-one
https://huagongshe.com/reaction/1973671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimedone | HCID 31358 | — |
| Reactant | HCID 3781742 | HCID 3781742 | — |
| Catalyst | Ammonium Acetate | HCID 517165 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 5,6,7,8-Tetrahydro-3,7,7-trimethylquinoline-5-one | HCID 4175192 | 41.2% |
Reaction Steps
A mixture of 3-amino-2-methylacrolein (8.5 g., 0.1 mol.) and dimedone (14 g., 0.1 mol.) was treated with triethylamine (5 ml.) and ammonium acetate (0.1 g.) and heated in an oil bath at 120° C with stirring for 20 hours. The cooled reaction mixture was diluted with 2N HCl (50 ml.) and extracted with ethyl acetate (2 × 50 ml.) and the extracts discarded. The aqueous solution was adjusted to pH 10.0 with sodium carbonate and extracted with ethyl acetate (3 × 50 ml.). The combined extracts were dried (MgSO4 and the solvent removed to give a residual oil which was distilled to give the title compound as a colourless oil (7.8 g., 40%) b.p. 80°/0.2 mm Hg. (RT = 2 min. 2% OV17, T=150°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03998831 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-2eb50403f1ea4f37991e7a31d3444d40 |
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| Source note | uspto-grants-1976_12 |
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