Reaktion #54840
ord-3d9256a617834f628b42d114deddc829
Reaktionsgleichung
piperidine
hydrochloric acid
3-Chloro-4-cyclohexylbenzaldehyde
malonic acid
malonic acid
→
3-chloro-4-cyclohexylcinnamic acid
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigefor 4 hours
- 2Temperaturthe mixture is refluxed for 1 hour
- 3Temperaturcooled
- 4workup.STIRRINGwith stirring
- 5FiltrationThe crystals of product are collected by filtration
- 6Waschenwashed with water (4× 150 ml) and air
- 7Sonstigedried
- 8SonstigeRecrystallization 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.