Potassium Carbonate → (R)-3-(2-bromopyridine-3-yloxy)-2-methyl-1-propanol
Reaktionsgleichung
[Br:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][N:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:16][C@H:17]([CH3:20])[CH2:18][OH:19]>CC(CC)=O>[Br:1][C:2]1[C:7]([O:8][CH2:16][C@H:17]([CH3:20])[CH2:18][OH:19])=[CH:6][CH:5]=[CH:4][N:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
2-bromo-3-pyridinol (230 mg) and potassium carbonate (216 mg) was dissolved in methylethylketone (10 ml) and reacted for 30 minutes. Then, (R)-3-bromo-2-methyl-1-propanol (0.21 ml) was added to the solution and refluxed for 3 hours at 100° C. Potassium carbonate was filtered out and separated by flash chromatography under a silica gel phase (ethyl acetate:normal hexane=1:1). As a result, (R)-3-(2-bromopyridine-3-yloxy)-2-methyl-1-propanol (260 mg, yield: 80%) was obtained.
Aufarbeitung
- customreacted for 30 minutes
- filtrationPotassium carbonate was filtered out
- customseparated by flash chromatography under a silica gel phase (ethyl acetate:normal hexane=1:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-5fa2f4940eee4c5b8f3328438231e505
- Quelldatensatz
- uspto-grants-2005_09
- Patentnummer
- US06946558B2
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