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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295276Generated: November 1, 2026

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

https://huagongshe.com/reaction/1295276

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), active manganese dioxide (30.00 g) and tetrahydrofuran (300 ml) was stirred overnight at room temperature. Insoluble material was filtered off and the filtrate was concentrated. The residue was subjected to silica gel column chromatography, and 3-benzyloxy-1-phenyl-1H-pyrazole-5-carbaldehyde (10.10 g, yield 91%) was obtained as a pale-yellow oil from a fraction eluted with ethyl acetate-hexane (1:2, volume ratio).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-152ec01c6cf24cde9281a8f9051a98cd
Source noteuspto-grants-2007_07