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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221619Generated: November 1, 2026

(3-amino-1-phenyl-1H-pyrazol-4-yl)methanol → 3-amino-1-phenyl-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/2221619

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-amino-1-phenyl-1H-pyrazol-4-yl)methanolHCID 23076463—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product3-amino-1-phenyl-1H-pyrazole-4-carbaldehydeHCID 2307661182.4%

Reaction Steps

A mixture of (3-amino-1-phenyl-1H-pyrazol-4-yl)methanol (12.29 g), activated manganese dioxide (35 g) and tetrahydrofuran (200 mL) was stirred at room temperature for 16 hrs. The reaction mixture was filtered, and the filtrate was concentrated. Recrystallization of the residue from tetrahydrofuran-hexane gave 3-amino-1-phenyl-1H-pyrazole-4-carbaldehyde as pale-yellow crystals (10.02 g, yield 82%). melting point: 129-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-beb7c6aaacdc48baa96767af1f113749
Source noteuspto-grants-2008_05