Acetyl chloride → Methyl (6-chloropyridin-3-yl)acetate
Reaktionsgleichung
[C:1](Cl)(=O)C.[Cl:5][C:6]1[N:11]=[CH:10][C:9]([CH2:12][C:13]([OH:15])=[O:14])=[CH:8][CH:7]=1>CO>[Cl:5][C:6]1[N:11]=[CH:10][C:9]([CH2:12][C:13]([O:15][CH3:1])=[O:14])=[CH:8][CH:7]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred solution of MeOH (25 mL) was added slowly acetyl chloride (3.5 mL). After 30 min, 2-(6-chloropyridin-3-yl)acetic acid (2.5 g) was added and the resulting reaction mixture stirred at room temperature for 2 hr. Solvents were then removed. The residue was dissolved in EtOAc and washed with 10% NaHCO3. The organic phase was dried and concentrated to afford the product (2.5 g).
Aufarbeitung
- customthe resulting reaction mixture
- customSolvents were then removed
- dissolutionThe residue was dissolved in EtOAc
- washwashed with 10% NaHCO3
- customThe organic phase was dried
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-94b96c9fade74805bc5e949afb46d2c8
- Quelldatensatz
- uspto-grants-2015_05
- Patentnummer
- US09040504B2
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