HCID 86739281, compound → 1,3,3,5,6-Pentamethylbicyclo[2.2.2]oct-5-en-2-one

HRID 1981276Notes

Reaction equation

HRID 1981276 reaction equation
C(O)(=O)C.C(O)(=O)C.O[CH2:10][C:11]1[CH:12]2[CH:20]=[CH:19][C:15]([CH3:21])([C:16]=1[CH2:17]O)[C:14](=[O:22])[C:13]2([CH3:24])[CH3:23]>[Pd].C(O)(C)C>[CH3:21][C:15]12[CH2:19][CH2:20][CH:12]([C:11]([CH3:10])=[C:16]1[CH3:17])[C:13]([CH3:24])([CH3:23])[C:14]2=[O:22]

Participants

4

Conditions

Temperature
80 °C

Procedure

To a 450 ml Parr mini-pressure reactor is charged 15 grams of 5,6-bis(hydroxymethyl)-1,3,3-trimethylbicyclo[2.2.2]-octa-5,7-dien-2-one diacetate produced according to Example IV, 60 ml of isopropyl alcohol and 0.3 grams of 10% palladium on charcoal. After flushing with nitrogen and hydrogen, the hydrogen is charged to a pressure of 195 psig while maintaining the reaction mass temperature at 22°-27° C. Within four minutes, the pressure drops to 140 psig and holds steady for six minutes. Hydrogen is again charged to 195 psig and the temperature is gradually raised to 80° C. At 80° C. the pressure beings to drop. The temperature is raised to 85° C. and maintained at 85° C. until the pressure holds constant at 102 psig (1.7 hours). After cooling to room temperature, the reaction mass is filtered and the toluene is removed in vacuo to yield 10.1 grams of 1,3,3,5,6-pentamethyl-bicyclo[2.2.2]octa-5-en-2-one. This material is identical to that prepared from 2,6,6-trimethylcyclohexa-2,4-dien-1-one and 2-butyne according to Examples I and II, supra.

Workup

  1. customproduced
  2. customAfter flushing with nitrogen and hydrogen
  3. additionthe hydrogen is charged to a pressure of 195 psig
  4. temperaturewhile maintaining the reaction mass temperature at 22°-27° C
  5. waitholds steady for six minutes
  6. additionHydrogen is again charged to 195 psig
  7. customAt 80° C.
  8. temperatureThe temperature is raised to 85° C.
  9. temperaturemaintained at 85° C. until the pressure
  10. customholds constant at 102 psig (1.7 hours)
  11. temperatureAfter cooling to room temperature
  12. filtrationthe reaction mass is filtered
  13. customthe toluene is removed in vacuo

Sources & evidence

ORD record
ord-ee5db5147f6248d997fed2e1fb0b474e
Source dataset
uspto-grants-1985_04
Patent number
US04514324

Reaction notes

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