Water → Phenol, 2,3-dimethyl-4-(phenylmethoxy)-
Reaktionsgleichung
[CH2:1](Br)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:9]([O-:12])([O-])=O.[K+].[K+].[OH2:15]>CN(C=O)C>[CH2:1]([O:15][C:3]1[CH:4]=[CH:5][C:9]([OH:12])=[C:7]([CH3:6])[C:2]=1[CH3:1])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 120 °C
Versuchsvorschrift
A mixture of 2,3-dimethyl-1,4-dihydroquinone (5 g) and benzyl bromide (6.2 g) and K2CO3 (10 g) in DMF (50 mL) was stirred at 120° C. for 5 h. The mixture was poured into water and extracted with EtOAc. The EtOAc was washed with water, dried and evaporated. The residue was purified by silica gel column eluting with 10% EtOAc in hexane to give 3.2 g of 4-benzyloxy-2,3-dimethyl-phenol as a pale solid.
Aufarbeitung
- extractionextracted with EtOAc
- washThe EtOAc was washed with water
- customdried
- customevaporated
- customThe residue was purified by silica gel column
- washeluting with 10% EtOAc in hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-843271ad65f94a439d31ea758f985c97
- Quelldatensatz
- uspto-grants-2009_08
- Patentnummer
- US07576094B2
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