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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1030695Erstellt: 26. Oktober 2026

Dimethylformamide → 3,4-Bis(methoxymethoxy)benzaldehyde

https://huagongshe.com/reaction/1030695

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktChloromethyl Methyl EtherHCID 7864—
Edukt3,4-DihydroxybenzaldehydeHCID 8768—
EduktDiisopropylethylamineHCID 81531—
Produkt3,4-Bis(methoxymethoxy)benzaldehydeHCID 1174631486,37%

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

In 200 ml of dimethylformamide was dissolved 32.66 g of 3,4-dihydroxybenzaldehyde, and the solution was cooled to -5° C. and 200 ml of N,N-diisopropylethylamine was added to the solution. Then, 70 ml of chloromethyl methyl ether was gradually added to the mixture, and the mixture was stirred overnight to effect reaction. After the reaction, the reaction mixture was poured into ice water, and the mixture was extracted with ethyl acetate three times. The organic layer was washed with water three times and shaken with a saturated aqueous solution of sodium chloride, and the organic layer was dried with anhydrous sodium sulfate and filtered. The solvent was removed from the filtrate by distillation, and the obtained residue was recrystallized from ethyl acetate to obtain 41.20 g (yield=86.37%) of 3,4-bis(methoxymethoxy)benzaldehyde.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05106871
Quelldatensatzuspto-grants-1992_04
ORD IDord-bb344d3643774669b01f31d879d4a6fa
Quellennotizuspto-grants-1992_04