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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349938Generated: October 30, 2026

(1-benzyl-3-benzyloxy-1H-pyrazol-4-yl)methanol → 1-benzyl-3-(benzyloxy)-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/349938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-benzyl-3-benzyloxy-1H-pyrazol-4-yl)methanolHCID 22930765—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product1-benzyl-3-(benzyloxy)-1H-pyrazole-4-carbaldehydeHCID 2293076890%

Reaction Steps

A mixture of (1-benzyl-3-benzyloxy-1H-pyrazol-4-yl)methanol (14.70 g), activated manganese dioxide (30.00 g), and tetrahydrofuran (200 ml) was stirred at room temperature for 2 hours. After the manganese dioxide was removed by filtration, the filtrate was concentrated. The crystals obtained were collected by filtration to yield 1-benzyl-3-benzyloxy-1H-pyrazole-4-carbaldehyde (13.10 g, yield: 90%). This was recrystallized from tetrahydrofuran-hexane. Melting point: 85–86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-4573e56c154348ed80950db373df823f
Source noteuspto-grants-2007_02