HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
p-Fluoronitrobenzene → 1-[2,4-Bis(methoxymethoxy)-6-(4-nitrophenoxy)phenyl]ethanone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | p-Fluoronitrobenzene | HCID 9590 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1-[2-Hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanone | HCID 10879697 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-[2,4-Bis(methoxymethoxy)-6-(4-nitrophenoxy)phenyl]ethanone | HCID 66759310 | 52% |
Reaktionsschritte
To a stirred suspension of 1-[2-hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanone (78 g, 298 mmol) and K2CO3 (45.3 g, 328 mmol) in DMSO (500 mL) and water (40 ml) was added 4-nitro-1-fluorobenzene (46.3 g, 328 mmol, 1.1 eq). After stirring for 15 min. at room temperature, the resulting suspension was heated for 6 hours at 55° C. After cooling, the dark solution was diluted with ethyl acetate (2000 mL) and thoroughly washed with 10% citric acid solution, then with brine and dried over Na2SO4. The solvent was removed and the residue was columned over silica gel eluting with cyclohexane/ethyl acetate 3/1, to provide the title compound (56 g, 52% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08993556B2 |
| Quelldatensatz | uspto-grants-2015_03 |
| ORD ID | ord-e370b93d25df41e0848e26659099a52e |
| Quellennotiz | uspto-grants-2015_03 |