Methanol → HCID 90389409, Verbindung
Reaktionsgleichung
[OH:1][C:2]1[CH:3]=[C:4]([CH3:11])[C:5]([C:8]([OH:10])=[O:9])=[N:6][CH:7]=1.S(=O)(=O)(O)O.[CH3:17]O>>[OH:1][C:2]1[CH:3]=[C:4]([CH3:11])[C:5]([C:8]([O:10][CH3:17])=[O:9])=[N:6][CH:7]=1Komponenten
Reaktionsbedingungen
- Temperatur
- 95 °C
Versuchsvorschrift
A sealable reaction vessel was charged with 5-hydroxy-3-methylpicolinic acid (0.651 g, 4.25 mmol) and MeOH (35 mL). The reaction vessel was placed in a water bath, and concentrated sulfuric acid (0.854 mL, 15.94 mmol) was added. The vessel was sealed and heated in a 95° C. oil bath. After 24 h, the reaction mixture was concentrated and the residue was taken up in 30 mL of 0.5M aqueous Na2CO3. The aqueous phase was extracted with 10% MeOH-EtOAc (100 mL). The aqueous layer was separated and saturated with NaCl. The aqueous phase was extracted with 10% MeOH-EtOAc (7×100 mL). The combined organic fractions were dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography, eluting with 3% to 4% MeOH-DCM to afford the title compound (593 mg). MS m/z=168 (M+H)+.
Aufarbeitung
- customThe reaction vessel was placed in a water bath
- customThe vessel was sealed
- concentrationthe reaction mixture was concentrated
- extractionThe aqueous phase was extracted with 10% MeOH-EtOAc (100 mL)
- customThe aqueous layer was separated and saturated with NaCl
- extractionThe aqueous phase was extracted with 10% MeOH-EtOAc (7×100 mL)
- dry with materialThe combined organic fractions were dried over MgSO4
- concentrationconcentrated
- customThe residue was purified by silica gel chromatography
- washeluting with 3% to 4% MeOH-DCM
Quellen und Nachweise
- ORD-Eintrag
- ord-63c654d5b8e44620a801f696a18bec73
- Quelldatensatz
- uspto-grants-2015_07
- Patentnummer
- US09085576B2
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