HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1388537Erstellt: 26. Oktober 2026
Dimethylformamide → 2-(2,5-Difluorophenylthio)-5-methoxy-benzaldehyde
https://huagongshe.com/reaction/1388537
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Bromo-5-methoxybenzaldehyde | HCID 344480 | — |
| Edukt | 2,5-Difluorobenzene-1-thiol | HCID 3836323 | — |
| Katalysator | Copper | HCID 23978 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-(2,5-Difluorophenylthio)-5-methoxy-benzaldehyde | HCID 12815952 | 52% |
Reaktionsschritte
A mixture of 19.7 g of 2-bromo-5-methoxybenzaldehyde (of Example 9, reference above), 14.1 g of 2,5-difluorothiophenol (of Example 11, reference above), 14.0 g of potassium carbonate, 75 ml dimethylformamide and 2.1 g of copper catalyst is stirred and heated to 150° C. for 6 hours. It is then diluted with 150 ml of water and extracted with benzene. The extract is washed with water, dried with magnesium sulfate and evaporated. The residue is processed by distillation. There are obtained 13.3 g (52%) of 2-(2,5-difluorophenylthio)-5-methoxy-benzaldehyde boiling at 163°-165° C./40 Pa. The product is crystallized from cyclohexane and melts in a pure state at 67°-68° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04431808 |
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| Quelldatensatz | uspto-grants-1984_02 |
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| ORD ID | ord-0f3fefc692ba4cd192befc23e910e4a9 |
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| Quellennotiz | uspto-grants-1984_02 |
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