HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1030695Erstellt: 26. Oktober 2026
Dimethylformamide → 3,4-Bis(methoxymethoxy)benzaldehyde
https://huagongshe.com/reaction/1030695
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Chloromethyl Methyl Ether | HCID 7864 | — |
| Edukt | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Produkt | 3,4-Bis(methoxymethoxy)benzaldehyde | HCID 11746314 | 86,37% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05106871 |
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| Quelldatensatz | uspto-grants-1992_04 |
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| ORD ID | ord-bb344d3643774669b01f31d879d4a6fa |
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| Quellennotiz | uspto-grants-1992_04 |
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