Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | N,N-Dimethylaniline | HCID 949 | — |
| Edukt | 2,5-Difluorophenol allyl ether | HCID 10749656 | — |
| Produkt | 2-Allyl-3,6-difluorophenol | HCID 10844863 | — |
Reaktionsschritte
The 2,5-difluorophenol allyl ether (13 g) was dissolved in N,N-dimethylaniline (90 ml) and the resulting solution was stirred under a nitrogen gas stream at 170° C. for 5 hr. Then the liquid reaction mixture was poured into a 10% aqueous solution of hydrogen chloride and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (developing solvent: 7% ethyl acetate/n-hexane) to give 2-allyl-3,6-difluorophenol (7.8 g) as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06258811B1 |
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| Quelldatensatz | uspto-grants-2001_07 |
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| ORD ID | ord-32e18329d084413c8c3d50c9c45f4cd1 |
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| Quellennotiz | uspto-grants-2001_07 |
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