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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295242Generated: November 2, 2026

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

https://huagongshe.com/reaction/1295242

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), active manganese dioxide (30.00 g) and tetrahydrofuran (200 ml) was stirred at room temperature for 2 hrs. Manganese dioxide was filtered off and the filtrate was concentrated. The obtained crystals were collected by filtration to give 1-benzyl-3-benzyloxy-1H-pyrazole-4-carbaldehyde (13.10 g, yield 90%). The crystals were recrystallized from tetrahydrofuran-hexane. melting point: 85–86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-cce858dfb159446babf6b675559e2a63
Source noteuspto-grants-2007_07