Hydrochloric Acid → 1-(2-Chloro-6-hydroxyphenyl)ethan-1-one
Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8]COC)[C:3]=1[C:12](=[O:14])[CH3:13].Cl>C1COCC1>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([OH:8])[C:3]=1[C:12](=[O:14])[CH3:13]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 65 °C
Versuchsvorschrift
To a solution of 1-(2-chloro-6-(methoxymethoxy)phenyl)ethanone (38 g, 177.03 mmol, 1.00 equiv) in THF (380 mL) was added HCl (aq. 35 g, 2.00 equiv, 36%). The resulting mixture was allowed to react, with stirring, for 3 h at 65° C. The resulting mixture was extracted with ethyl acetate. The organic phase was separated, dried and concentrated under vacuum to give the crude title compound.
Aufarbeitung
- customto react
- extractionThe resulting mixture was extracted with ethyl acetate
- customThe organic phase was separated
- customdried
- concentrationconcentrated under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-03868c8c1c2a46798ba082f6f08f4fe3
- Quelldatensatz
- uspto-grants-2015_10
- Patentnummer
- US09168248B2
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