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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839245Generated: October 31, 2026

[3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazol-4-yl]methanol → 3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/839245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazol-4-yl]methanolHCID 20326211—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product3-(5-Nitrofuran-2-yl)-1-phenyl-1H-pyrazole-4-carbaldehydeHCID 20326255—

Reaction Steps

Heat 0.42 g of 4-hydroxymethyl-3-(5-nitro-2-furyl)-1-phenylpyrazole with 1.3 g of activated manganese dioxide and 6 ml of chloroform for 4 hours at boiling with removal of water. Filter while warm and extract the filter residue three times by boiling with chloroform. Concentrate the produced organic solutions to obtain 3-(5-nitro-2-furyl)-1-phenylpyrazole-4-carboxaldehyde [m.p. 208° to 209° C].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04093812
Source datasetuspto-grants-1978_06
ORD IDord-94d09087271b4328a2c67bc52eba23b2
Source noteuspto-grants-1978_06