Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221654Generated: October 26, 2026

[3-(methylamino)-1-phenyl-1H-pyrazol-4-yl]methanol → 3-(methylamino)-1-phenyl-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/2221654

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-(methylamino)-1-phenyl-1H-pyrazol-4-yl]methanolHCID 69217492—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product3-(methylamino)-1-phenyl-1H-pyrazole-4-carbaldehydeHCID 23076364—

Reaction Steps

A mixture of [3-(methylamino)-1-phenyl-1H-pyrazol-4-yl]methanol (15.42 g), activated manganese dioxide (50 g) and tetrahydrofuran (150 mL) was stirred at room temperature for 16 hrs. The obtained mixture was filtered, and the filtrate was concentrated. The residue was subjected to silica gel column chromatography to give 3-(methylamino)-1-phenyl-1H-pyrazole-4-carbaldehyde as colorless crystals from a fraction eluted with ethyl acetate-hexane (1:4, v/v). Recrystallization from ethyl acetate-hexane gave colorless needle crystal (9.17 g, yield 60%). melting point: 83-84° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-d9459743dd9e4c50905fa4a369406992
Source noteuspto-grants-2008_05