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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720293Generated: October 31, 2026

Benzaldehyde → HCID 15290694, compound

https://huagongshe.com/reaction/1720293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHCID 22923703HCID 22923703—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 15290694HCID 1529069464.8%

Reaction Steps

27 g of 1-(2-aminoethyl)-4-methoxymethoxypiperidine was dropwise added to a solution of 15 g of benzaldehyde in 300 ml of ethanol, at room temperature. The mixture was stirred at the same temperature for 1 day. To the reaction mixture was added 5 g of 10% Pd-C, and the resulting mixture was allowed to absorb hydrogen at room temperature at atmospheric pressure. After a reaction was over, the catalyst was removed by filtration. The filtrate was diluted with ethyl acetate. The dilution was subjected to extraction with 10% hydrochloric acid. The aqueous layer was made alkaline with an aqueous potassium hydroxide solution and then subjected to extraction with ethyl acetate. The extract was washed with water and dried with magnesium sulfate. The solvent was removed by distillation. The resulting residue was purified by a silica gel column chromatography (eluant: 10% methanol-chloroform) to obtain 25.50 g of 1-(2-benzylaminoethyl)-4-methoxymethoxypiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506239
Source datasetuspto-grants-1996_04
ORD IDord-d354411db17146f5a59b7888d81cc6ae
Source noteuspto-grants-1996_04