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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488147Generated: October 28, 2026

Water → (E)-1-[3-(5-ethyl-4-hydroxy-3-methoxy-1-naphthyl)-1-oxo-2-propenyl]piperidine

https://huagongshe.com/reaction/488147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant5-Ethyl-3-methoxy-4-methoxymethoxy-1-naphthalenecarbaldehydeHCID 9970569—
ReactantDiethyl [2-oxo-2-(piperidin-1-yl)ethyl]phosphonateHCID 13203262—
SolventDimethylformamideHCID 6228—
Product(E)-1-[3-(5-ethyl-4-hydroxy-3-methoxy-1-naphthyl)-1-oxo-2-propenyl]piperidineHCID 14986482111.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298649
Source datasetuspto-grants-1994_03
ORD IDord-e41e6052f6274f1a9ff49ba561439c8f
Source noteuspto-grants-1994_03