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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413756Generated: November 2, 2026

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

https://huagongshe.com/reaction/1413756

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 numberUS04251454
Source datasetuspto-grants-1981_02
ORD IDord-955011b6099c40c7bdfc37de029e2cd0
Source noteuspto-grants-1981_02