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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158858Generated: November 5, 2026

{4H,5H,6H-pyrrolo[1,2-b]pyrazol-2-yl}methanol → 4H,5H,6H-pyrrolo(1,2-b)pyrazole-2-carbaldehyde

https://huagongshe.com/reaction/1158858

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{4H,5H,6H-pyrrolo[1,2-b]pyrazol-2-yl}methanolHCID 21941359—
CatalystManganese dioxideHCID 14801—
SolventChloroformHCID 6212—
Product4H,5H,6H-pyrrolo(1,2-b)pyrazole-2-carbaldehydeHCID 11286491—

Reaction Steps

MnO2 (activated) (24.4 g) was added to the CHCl3 (350 mL) solution of (5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-2-yl)methanol (4.87 g) and refluxed for 1 h under a nitrogen atmosphere. The reaction mixture was filtered through a pad of Celite. The filtrate was reduced under reduced pressure. The residue was applied to silica gel column chromatography, then the column was eluted with n-hexane-AcOEt (1/1-1/2). The title compound was obtained as yellow oil (4.35 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812014B2
Source datasetuspto-grants-2010_10
ORD IDord-174db0ed55454fdab55623d8c8603c9c
Source noteuspto-grants-2010_10