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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266784Generated: November 1, 2026

HCID 19030865, compound → HCID 19030736, compound

https://huagongshe.com/reaction/266784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19030865HCID 19030865—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
ProductHCID 19030736HCID 1903073683.3%

Reaction Steps

A mixture of N-(1-benzyl-4-piperidinyl)-o-hydroxymethylaniline (2.9 g), chloroform (100 ml) and manganese dioxide (12 g) is refluxed for 1 hour. After cooling, the mixture is filtered and the filtrate is concentrated. The resulting residue is purified by silica gel column chromatography (eluent; dichloromethane) to give N-(1-benzyl-4-piperidinyl)-o-formylaniline (2.4 g) as yellow powders, m.p. 87°-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652247
Source datasetuspto-grants-1997_07
ORD IDord-29eb229db1394b1e909d61f26fdf5343
Source noteuspto-grants-1997_07