Reaktionsgleichung
[OH:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[C:10](=[O:13])[CH2:11][CH3:12].C(=O)([O-])[O-].[K+].[K+].Br[CH2:21][CH2:22][O:23][CH3:24]>CN(C=O)C>[CH3:9][O:8][C:6]1[CH:5]=[CH:4][C:3]([C:10](=[O:13])[CH2:11][CH3:12])=[C:2]([O:1][CH2:21][CH2:22][O:23][CH3:24])[CH:7]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 1-(2-hydroxy-4-methoxyphenyl)propan-1-one (1 g, 5.55 mmol) in DMF (50 ml) is treated with potassium carbonate (0.920 g, 6.66 mmol) and stirred at RT for approximately 10 mins. 1-Bromo-2-methoxyethane (0.771 g, 5.55 mmol) is added and the mixture is stirred at RT overnight. The solvent is removed in vacuo and the residue is partitioned between in EtOAc/H2O. The organic phase is separated and washed with sat Na2CO3, 1M HCl, brine, dried (MgSO4) and concentrated in vacuo to afford a dark green/brown oil. Purification by chromatography on silica gel (50 g+70 g) eluting with 20% EtOAc/iso-hexane affords the title compound; MS m/z 239.2 [M+H]+.
Aufarbeitung
- stirringthe mixture is stirred at RT overnight
- customThe solvent is removed in vacuo
- customthe residue is partitioned between in EtOAc/H2O
- customThe organic phase is separated
- washwashed with sat Na2CO3, 1M HCl, brine
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customto afford a dark green/brown oil
- customPurification by chromatography on silica gel (50 g+70 g)
- washeluting with 20% EtOAc/iso-hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-5a16cbcca7664ac1b88171ef6a04dd0c
- Quelldatensatz
- uspto-grants-2011_08
- Patentnummer
- US07994203B2
Verknüpfte Notizen
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