Reaktion #54840

ord-3d9256a617834f628b42d114deddc829

Reaktionsgleichung

C1CCNCC1
piperidine
Cl
hydrochloric acid
O=Cc1ccc(C2CCCCC2)c(Cl)c1
3-Chloro-4-cyclohexylbenzaldehyde
O=C(O)CC(=O)O
malonic acid
O=C(O)CC(=O)O
malonic acid
O=C(O)C=Cc1ccc(C2CCCCC2)c(Cl)c1
3-chloro-4-cyclohexylcinnamic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigefor 4 hours
  2. 2
    Temperaturthe mixture is refluxed for 1 hour
  3. 3
    Temperaturcooled
  4. 4
    workup.STIRRINGwith stirring
  5. 5
    FiltrationThe crystals of product are collected by filtration
  6. 6
    Waschenwashed with water (4× 150 ml) and air
  7. 7
    Sonstigedried
  8. 8
    SonstigeRecrystallization from acetone-water

Vorschrift

3-Chloro-4-cyclohexylbenzaldehyde (0.1 mole), malonic acid (0.2 moles), and dry pyridine (175 ml) are placed in a 1 l round-bottom flask. The malonic acid is dissolved by shaking on a steam bath and piperidine (0.5 ml) is added. The reaction is allowed to take place on the steam bath for 4 hours. After standing at room temperature overnight, the mixture is refluxed for 1 hour and cooled. The reaction mixture is poured into 250 ml of ice water and acidified with concentrated hydrochloric acid (80 ml) with stirring. The crystals of product are collected by filtration, washed with water (4× 150 ml) and air dried. Recrystallization from acetone-water gives 3-chloro-4-cyclohexylcinnamic acid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04150148uspto-grants-1979_04