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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654724Generated: October 31, 2026

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

https://huagongshe.com/reaction/654724

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-3-methoxy-4-methoxymethoxy-1-naphthyl)-1-oxo-2-propenyl]piperidineHCID 1498647298.4%

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 numberUS05134111
Source datasetuspto-grants-1992_07
ORD IDord-6ac1a6224f3f4867adec52f6d704318f
Source noteuspto-grants-1992_07