HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39328Erstellt: 23. Oktober 2026
Chlorodifluoromethane → 4-(Difluoromethoxy)-3-hydroxybenzaldehyde
https://huagongshe.com/de/reaction/39328
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chlorodifluoromethane | HCID 6372 | — |
| Edukt | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(Difluoromethoxy)-3-hydroxybenzaldehyde | HCID 2758295 | 25% |
Reaktionsschritte
To a well stirred suspension of 3,4-dihydroxy benzaldehyde (100 gm) and anhydrous potassium carbonate (120 gm) in dry N,N-dimethylformamide (1.0 lit) was passed chlorodifluoromethane gas for about 30 minutes at about 80-85° C. After an hour another lot of anhydrous potassium carbonate (25.0 gm) was added and stirred for about one and half hours. The third lot of anhydrous potassium carbonate (25.0 gm) was added and stirred for about one and half hours. The reaction mixture was then stirred for about 5-6 hours at an ambient temperature. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The residue obtained was diluted with water (500 mL) and extracted with ethyl acetate (3×200 mL). The combined organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude product obtained was purified through silica gel column to give 4-difluoromethoxy-3-hydroxy benzaldehyde.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524905B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-ac21ed1fc5ba469eb3bf2c9a44f79dad |
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| Quellennotiz | uspto-grants-2013_09 |
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