Reaktionsgleichung
[F:1][C:2]1[C:3]([OH:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].S(Cl)(Cl)=O.[CH3:16]O>>[F:1][C:2]1[C:3]([OH:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([O:7][CH3:16])=[O:6]Komponenten
4
Reaktionsbedingungen
- Temperatur
- 40 °C
Versuchsvorschrift
To a solution of 3-fluoro-2-hydroxy-benzoic acid (5.0 g, 32 mmol) in methanol (20 mL) was added thionyl chloride (5.0 g, 42 mmol) dropwise and the reaction mixture was stirred at 40° C. for 3 hours, then heated at 50° C. for 16 hours. The reaction mixture was cooled and concentrated in vacuo and resulting residue was purified by silica gel column chromatography using 0-50% ethyl acetate/hexanes mixtures as eluant to give methyl 3-fluoro-2-hydroxy-benzoate (5.1 g, 94%) as white crystals. ESI-MS m/z calc. 170.0. Found 170.9 (M+1)+; Retention time: 1.33 minutes (3 min run).
Aufarbeitung
- temperatureheated at 50° C. for 16 hours
- temperatureThe reaction mixture was cooled
- concentrationconcentrated in vacuo
- customresulting residue
- customwas purified by silica gel column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-69bec4cc329b42299e5d64fc6c767f2f
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08828996B2
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