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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221663Generated: October 30, 2026

Chloromethyl Methyl Ether → 3-(methoxymethoxy)-1-phenyl-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/2221663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178519806HCID 178519806—
SolventTetrahydrofuranHCID 8028—
Product3-(methoxymethoxy)-1-phenyl-1H-pyrazole-4-carbaldehydeHCID 2307651358%

Reaction Steps

A mixture of 3-hydroxy-1-phenyl-1H-pyrazole-4-carbaldehyde (1.88 g), chloromethyl methyl ether (0.835 mL), N,N-diisopropylethylamine (2.09 mL) and tetrahydrofuran (30 mL) was stirred at room temperature for 2 hrs. Saturated aqueous sodium hydrogen carbonate was poured into the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was washed with diisopropyl ether-hexane to give 3-(methoxymethoxy)-1-phenyl-1H-pyrazole-4-carbaldehyde as white crystals (1.34 g, yield 58%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 106-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-cd474026754942c88a04e9bb6559bb96
Source noteuspto-grants-2008_05