Water → 1-(Allyloxy)-4-methyl-2-nitrobenzene
Reaktionsgleichung
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1.Br[CH2:13][CH:14]=[CH2:15].C([O-])([O-])=O.[K+].[K+].O>CC(C)=O>[CH2:15]([O:8][C:5]1[CH:6]=[CH:7][C:2]([CH3:1])=[CH:3][C:4]=1[N+:9]([O-:11])=[O:10])[CH:14]=[CH2:13]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 4-methyl-2-nitrophenol (5.0 g, 0.033 mol), 3-bromoprop-1-ene (4.2 g, 0.034 mol) and K2CO3 (4.6 g, 0.033 mol) in acetone (20 mL) was stirred for 8 h at ambient temperature. The mixture was poured into water (50 mL), extracted with EtOAc (90 mL), washed with brine, dried and concentrated to give the title compound (7a).
Aufarbeitung
- extractionextracted with EtOAc (90 mL)
- washwashed with brine
- customdried
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-e9d414ef53804be9ad7bc425ba6670d4
- Quelldatensatz
- uspto-grants-2015_12
- Patentnummer
- US09206166B2
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