HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3,4-Dihydroxybenzaldehyde → 4-(Difluoromethoxy)-3-hydroxybenzaldehyde
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Methyl chlorodifluoroacetate | HCID 73935 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(Difluoromethoxy)-3-hydroxybenzaldehyde | HCID 2758295 | 38% |
Reaktionsschritte
3,4-Dihydroxybenzaldehyde (0.50 g, 3.62 mmol, Aldrich), methyl chlorodifluoroacetate (0.52 g, 3.62 mmol, Aldrich) and potassium carbonate (0.50 g, 3.62 mmol) were combined in DMF (5.0 mL) under an argon atmosphere. After stirring at 60°-65° C. for 3 h, DMF was removed in vacuo and the residue was partioned between aqueous 3N HCl and ether. The aqueous layer was extracted three times with ether. The combined organic extracts were washed with water, with brine, were dried (MgSO4), filtered and evaporated. The residue was purified by flash chromatography (silica gel, 25% ethyl acetate/hexanes) to provide the title compound as a white solid (0.20 g, 38%). mp 83°-85° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05731477 |
| Quelldatensatz | uspto-grants-1998_03 |
| ORD ID | ord-e57e5ba30ba5446d9ef33fda5e7bc0ab |
| Quellennotiz | uspto-grants-1998_03 |