Reacción #531801

ord-860b0fec791542ebb28cf35cbda460b7

Ecuación de reacción

O=C(O)CCC(=O)c1cc2ccc3ccc4ccc5ccc6ccc1c1c6c5c4c3c21
compound 82
O=C(O)CCC(=O)c1cc2ccc3ccc4ccc5ccc6ccc1c1c6c5c4c3c21
γ-oxo-4-(coronen-1-yl)butanoic acid
NN
hydrazine
[Na+].[OH-]
sodium hydroxide
O=C(O)CCCc1cc2ccc3ccc4ccc5ccc6ccc1c1c6c5c4c3c21
brownish-red solid
Rendimiento 88.5%
O=C(O)CCCc1cc2ccc3ccc4ccc5ccc6ccc1c1c6c5c4c3c21
4-(coronen-1-yl)butanoic acid
Rendimiento 88.5%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITfollowed by 90-minute
  2. 2
    Temperaturarefluxing in a 180-° C
  3. 3
    workup.DISTILLATIONThe excess hydrazine and water were distilled away
  4. 4
    Otroto precipitate a solid substance
  5. 5
    FiltraciónThe solid substance was collected by filtration
  6. 6
    Lavadowas washed with ion-exchange water
  7. 7
    Otroby drying under reduced pressure
  8. 8
    workup.ADDITIONThis solid substance was dispersed in 10 ml of xylene
  9. 9
    Temperaturawas heated to 140° C
  10. 10
    workup.DISSOLUTIONIn this manner, the solid substance was dissolved
  11. 11
    TemperaturaAfter that, the substance was cooled slowly back to room temperature
  12. 12
    Otroto precipitate a solid substance
  13. 13
    FiltraciónThe solid substance generated here was collected by filtration
  14. 14
    Otrowas dried under reduced pressure

Procedimiento

The compound 82 (0.503 g, 1.26 mmol), 0.4 ml of 79% aqueous hydrazine, and 0.462 g (11.6 mmol) of sodium hydroxide were dissolved in 3.0 ml of diethylene glycol, followed by 90-minute refluxing in a 180-° C. oil bath. The excess hydrazine and water were distilled away, and the refluxing was continued for two more hours. After the reaction was completed, the solution was cooled back to room temperature, to precipitate a solid substance. The solid substance was collected by filtration, and was washed with ion-exchange water, followed by drying under reduced pressure. This solid substance was dispersed in 10 ml of xylene, and was heated to 140° C. In this manner, the solid substance was dissolved. After that, the substance was cooled slowly back to room temperature, to precipitate a solid substance. The solid substance generated here was collected by filtration, and was dried under reduced pressure, to obtain 0.431 g of the brownish-red solid substance 83. Here, 1HNMR was not measured, since its product was not soluble in any deuterated solvents.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08475685B2uspto-grants-2013_07