Reaktion #160126

ord-f42e4f4d409d4b4daff3a9df8d97d428

Reaktionsgleichung

O=C(O)c1ccc(O)cc1F
2-fluoro-4-hydroxy-benzoic acid
O=S(Cl)Cl
thionyl chloride
CO
methanol
COC(=O)c1ccc(O)cc1F
methyl 2-fluoro-4-hydroxy-benzoate
Ausbeute 40.0%

Reaktionsbedingungen

Temperatur
40°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe reaction mixture was concentrated in vacuo
  2. 2
    workup.ADDITIONdiluted with DCM (100 mL)
  3. 3
    Waschenwashed with aqueous saturated NaHCO3 (2×50 mL) solution
  4. 4
    SonstigeThe organics were separated
  5. 5
    Trocknendried with MgSO4
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated in vacuo

Vorschrift

To a solution of 2-fluoro-4-hydroxy-benzoic acid (5.32 g, 34.1 mmol) in methanol (21 mL) was added thionyl chloride (4.86 g, 3 mL, 40.9 mmol) dropwise and the reaction mixture was stirred at 40° C. for 3 hours. The reaction mixture was concentrated in vacuo and diluted with DCM (100 mL) and washed with aqueous saturated NaHCO3 (2×50 mL) solution. The organics were separated and dried with MgSO4, filtered and concentrated in vacuo to give methyl 2-fluoro-4-hydroxy-benzoate (2.3 g, 40%). ESI-MS m/z calc. 170.1. Found 171.3 (M+1)+; Retention time: 0.84 minutes (3 min run).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08828996B2uspto-grants-2014_09