HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (E)-1-[3-(5-ethyl-4-hydroxy-3-methoxy-1-naphthyl)-1-oxo-2-propenyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Ethyl-3-methoxy-4-methoxymethoxy-1-naphthalenecarbaldehyde | HCID 9970569 | — |
| Reactant | Diethyl [2-oxo-2-(piperidin-1-yl)ethyl]phosphonate | HCID 13203262 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-1-[3-(5-ethyl-4-hydroxy-3-methoxy-1-naphthyl)-1-oxo-2-propenyl]piperidine | HCID 14986482 | 111.1% |
Reaction Steps
0.15 g of 60% sodium hydride was suspended in 20 ml of N,N-dimethylformamide, to which 1.15 g of N-(diethoxyphosphoryl)acetylpiperidine was gradually added at room temperature. After stirring for 10 minutes, a solution of 800 mg of 5-ethyl-3-methoxy-4-methoxymethoxy-1-naphthalenecarbaldehyde in N,N-dimethylformamide (10 ml) was gradually added. After stirring for 20 minutes, water was added, followed by extraction with ethyl acetate. The combined extracts were washed with water and dried over anhydrous magnesium sulfate. After removal of the solvent, the resultant residue was purified by silica gel column chromatography (30% ethyl acetate/hexane) to obtain 1.1 g of the titled compound as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05298649 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-e41e6052f6274f1a9ff49ba561439c8f |
| Source note | uspto-grants-1994_03 |