HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoylacetone → 1-phenyl-2-piperidin-2-ylidenebutane-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoylacetone | HCID 7166 | — |
| Reactant | 2-Ethoxy-3,4,5,6-tetrahydropyridine | HCID 12210255 | — |
| Product | 1-phenyl-2-piperidin-2-ylidenebutane-1,3-dione | HCID 178467972 | — |
Reaction Steps
12.7 g (0.1 mole) of 2-ethoxy-3,4,5,6-tetrahydropyridine and 24.4 g (0.15 mole) of 1-phenyl-1,3-butanedione are mixed and heated together in a nitrogen atmosphere, with stirring, for 32 hours in an oil bath at 100°. The reaction mixture is cooled, and subsequently chromatographed on silica gel with an ethyl acetate/hexane mixture as the eluant. The main fractions are combined and crystallised from ether to obtain 1-phenyl-2-(2-piperidinylidene)-1,3-butanedione in the form of yellow crystals, m.p. 80°-81°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04130652 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-b80ae327a1504a2aa6409de3523f995e |
| Source note | uspto-grants-1978_12 |