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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295221Generated: October 31, 2026

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

https://huagongshe.com/reaction/1295221

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-benzyloxy-1-methyl-1H-pyrazol-4-yl)methanolHCID 22930776—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product3-(benzyloxy)-1-methyl-1H-pyrazole-4-carbaldehydeHCID 2293072381.2%

Reaction Steps

A mixture of (3-benzyloxy-1-methyl-1H-pyrazol-4-yl)methanol (18.40 g), active manganese dioxide (40.00 g) and tetrahydrofuran (200 ml) was stirred at room temperature for 9 hrs. Manganese dioxide was filtered off and the filtrate was concentrated. The residue was subjected to silica gel column chromatography, and 3-benzyloxy-1-methyl-1H-pyrazole-4-carbaldehyde (14.80 g, yield 81%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (2:1, volume ratio).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-94b8d23fa42d4fce93be60b37627eca5
Source noteuspto-grants-2007_07