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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221612Generated: October 31, 2026

(3-benzyloxy-1-phenyl-1H-pyrazol-5-yl)methanol → HCID 22930766, compound

https://huagongshe.com/reaction/2221612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-benzyloxy-1-phenyl-1H-pyrazol-5-yl)methanolHCID 22930692—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22930766HCID 2293076691%

Reaction Steps

A mixture of (3-benzyloxy-1-phenyl-1H-pyrazol-5-yl)methanol (11.20 g), activated manganese dioxide (30.00 g) and tetrahydrofuran (300 mL) was stirred overnight at room temperature. The insoluble material was removed by filtration, and the mother liquid was concentrated. The residue was subjected to silica gel column chromatography to give 3-benzyloxy-1-phenyl-1H-pyrazole-5-carbaldehyde (10.10 g, yield 91%) as a pale-yellow oil from a fraction eluted with ethyl acetate-hexane (1:2, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-4e3ba7244554440e8361a27aae44d5df
Source noteuspto-grants-2008_05