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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441325Generated: October 30, 2026

[3,5-Bis(dimethylamino)-4-(piperidin-1-yl)phenyl]methanol → 3,5-Bis(dimethylamino)-4-(piperidin-1-yl)benzaldehyde

https://huagongshe.com/reaction/441325

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3,5-Bis(dimethylamino)-4-(piperidin-1-yl)phenyl]methanolHCID 53863713—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product3,5-Bis(dimethylamino)-4-(piperidin-1-yl)benzaldehydeHCID 20290402—

Reaction Steps

12.9 G. of 3,5-bis(dimethylamino)-4-piperidinobenzyl alcohol, 17.1 g. of activated manganese dioxide and 80 ml. of chloroform were mixed together and stirred at room temperature for 48 hours. The manganese dioxide was filtered off, washed with chloroform and the chloroform evaporated. After purification over aluminum oxide with benzene and recrystallization from ethanol, there was obtained 3,5-bis(dimethylamino)-4-piperidinobenzaldehyde having a melting point of 114°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04039543
Source datasetuspto-grants-1977_08
ORD IDord-0844605f208945f1bbb0e91e5550e7a6
Source noteuspto-grants-1977_08