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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32248Generated: October 26, 2026

[4-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)phenyl]methanol → 4-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzaldehyde

https://huagongshe.com/reaction/32248

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[4-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)phenyl]methanolHCID 23142118—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product4-(4-t-Butylcyclohexyl)-3-(4-butylpiperazin-1-yl)benzaldehydeHCID 2314250085.1%

Reaction Steps

A mixture of the crude product of [4-(4-t-butylcyclohexyl)-3-(4-butylpiperazin-1-yl)phenyl]methanol produced in Example (101a) (294 mg), manganese (IV) oxide (1.3 g, 14.95 mmol) and chloroform (15 mL) was refluxed for 40 minutes. The reaction mixture was filtered and insoluble materials were filtered off. The filtrate was concentrated under reduced pressure to give 249 mg of a crude product of the title compound as an ochre oil. This product was directly used without purification for the following reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425554B2
Source datasetuspto-grants-2008_09
ORD IDord-449de0b95d344595ad9297220a8b494d
Source noteuspto-grants-2008_09