Benzyl Bromide → Methyl 2-(4-(benzyloxy)-3-bromophenyl)acetate
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([O:12][CH3:13])=[O:11])[CH:5]=[CH:6][C:7]=1[OH:8].C(=O)([O-])[O-].[K+].[K+].[CH2:20](Br)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>CC(C)=O>[Br:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([O:12][CH3:13])=[O:11])[CH:5]=[CH:6][C:7]=1[O:8][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Compound 10 (12.3 g) was dissolved in 100 mL acetone and 7.6 g of potassium carbonate was added. 8.6 g of benzyl bromide was added with stirring. The solid was removed by suction filtration and the liquid was evaporated to product 11.
Aufarbeitung
- customThe solid was removed by suction filtration
- customthe liquid was evaporated to product 11
Quellen und Nachweise
- ORD-Eintrag
- ord-d183db3ee6454f69b0c850e9b2968b79
- Quelldatensatz
- uspto-grants-2016_06
- Patentnummer
- US09359372B2
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