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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221574Generated: November 1, 2026

Vanillin → HCID 86605716, compound

https://huagongshe.com/reaction/2221574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVanillinHCID 1183—
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant[3-Methyl-1-(pyridin-2-yl)-1H-pyrazol-4-yl]methanolHCID 23076503—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86605716HCID 8660571677.5%

Reaction Steps

To a mixture of (3-methyl-1-pyridin-2-yl-1H-pyrazol-4-yl)methanol (1.07 g), vanillin (0.85 g), tributylphosphine (1.70 g) and tetrahydrofuran (100 mL) as added 1,1′-(azodicarbonyl)dipiperidine (2.12 g) at room temperature, and the mixture was stirred for 15 hrs. The precipitated crystals were removed by filtration. The filtrate was concentrated and the residue was subjected to silica gel column chromatography to give 3-methoxy-4-[(3-methyl-1-pyridin-2-yl-1H-pyrazol-4-yl)methoxy]benzaldehyde as colorless crystals (1.40 g, yield 77%) from a fraction eluted with ethyl acetate-hexane (1:1, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 141-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-a73991e8d5e944e589ecac6bae551e04
Source noteuspto-grants-2008_05