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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295270Generated: October 30, 2026

HCID 69218567, compound → 3-[4-[2-(2-furyl)-5-methyl-4-oxazolylmethoxy]-3-methoxybenzyloxy]-1-phenyl-1H-pyrazole-5-carbaldehyde

https://huagongshe.com/reaction/1295270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69218567HCID 69218567—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
Product3-[4-[2-(2-furyl)-5-methyl-4-oxazolylmethoxy]-3-methoxybenzyloxy]-1-phenyl-1H-pyrazole-5-carbaldehydeHCID 8659167177%

Reaction Steps

A mixture of [3-[4-[2-(2-furyl)-5-methyl-4-oxazolylmethoxy]-3-methoxybenzyloxy]-1-phenyl-1H-pyrazol-5-yl]methanol (9.50 g), active manganese dioxide (30.00 g) and tetrahydrofuran (300 ml) was stirred at room temperature for 15 hrs. Manganese dioxide was filtered off and the filtrate was concentrated. The residue was subjected to silica gel column chromatography, and 3-[4-[2-(2-furyl)-5-methyl-4-oxazolylmethoxy]-3-methoxybenzyloxy]-1-phenyl-1H-pyrazole-5-carbaldehyde (7.27 g, yield 77%) was obtained as colorless crystals from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). The crystals were recrystallized from ethyl acetate-hexane. melting point: 103–104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-6a7f74f2b2a84d71be32769eabf3e140
Source noteuspto-grants-2007_07