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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976127Generated: October 29, 2026

1-Benzylpiperidine-4-carbaldehyde → HCID 54153280, compound

https://huagongshe.com/reaction/976127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzylpiperidine-4-carbaldehydeHCID 89584—
ReactantHCID 19968934HCID 19968934—
ReactantSodium methanolate methanolHCID 23694274—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54153280HCID 5415328040.6%

Reaction Steps

Under ice cooling, 1.70 g of a 28% sodium methoxide·methanol solution was added to 1.96 g of 4-(1-oxoindan-5-yl)amino-5,6-dihydro-7H-cyclopenta[d]pyrimidine dissolved in tetrahydrofuran, and then 1.80 g of 1-benzyl-4-formylpiperidine was added dropwise thereto. After the mixture was stirred for 1.5 hours, a saturated saline solution was added to the reaction mixture, and the mixture was extracted with chloroform. The extract was dried over anhydrous sodium sulfate and condensed under reduced pressure. The obtained residue was applied to silica gel column chromatography and then recrystallized from chloroform to obtain 1.35 g of the title compound as pale yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05610303
Source datasetuspto-grants-1997_03
ORD IDord-2b315716a9d24b1b9b81ced558008e84
Source noteuspto-grants-1997_03