Reaktion #423409

ord-2230f89093db4e649b0bbaea6606ee11

Reaktionsgleichung

[Na+].[OH-]
NaOH
COC(=O)c1ccc(F)cc1
methyl 4-fluorobenzoate
C1CCNCC1
piperidine
[Li+].[OH-]
lithium hydroxide
O=C(O)c1ccc(N2CCCCC2)cc1
title compound
O=C(O)c1ccc(N2CCCCC2)cc1
4-Piperidin-1-ylbenzoic acid

Lösungsmittel

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe obtained solution evaporated in vacuo
  2. 2
    Sonstigeto give a colourless oil
  3. 3
    workup.STIRRINGThe reaction mixture was stirred at room temperature for 6 hours
  4. 4
    workup.WAITat 60° C. for 16 hours
  5. 5
    Temperaturthe reaction mixture was refluxed for 24 hours
  6. 6
    TemperaturAfter cooling
  7. 7
    Waschenwashed with Et2O
  8. 8
    Filtrationthe formed precipitate was collected by filtration
  9. 9
    Waschenwashed with water
  10. 10
    Sonstigedried under high vacuum

Vorschrift

A mixture of methyl 4-fluorobenzoate (Lancaster 14154; 500 mg; 3.24 mmol; 1 eq.) and piperidine (Fluka 80640; 828.62 mg; 9.73 mmol; 3 eq.) in DMF (2 mL) was stirred at 50° C. for 16 hours. The reaction mixture was then passed through a short pad of silica and the obtained solution evaporated in vacuo to give a colourless oil. The oil was taken up in THF (15 mL) and lithium hydroxide (388.41 mg; 16.22 mmol; 5 eq.) was added followed by water (15 mL). The reaction mixture was stirred at room temperature for 6 hours then at 60° C. for 16 hours. NaOH (155.5 mg, 6.48 mmol, 2 eq) was then added and the reaction mixture was refluxed for 24 hours. After cooling, the solution was diluted with water and washed with Et2O. The aqueous layer was then acidified to pH 5-6 with acetic acid and the formed precipitate was collected by filtration, washed with water and dried under high vacuum to afford the title compound as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08889668B2uspto-grants-2014_11