Isoprene → 1,4,6-Octatriene, 2,7-dimethyl-, (E)-

HRID 918223Notes

Reaction equation

HRID 918223 reaction equation
[CH2:1]=[CH:2][C:3](=[CH2:5])[CH3:4]>C/C(/[O-])=C/C(C)=O.C/C(/[O-])=C/C(C)=O.[Pd+2].C1(P(C2CCCCC2)C2CCCCC2)CCCCC1.P(=O)(O)(O)O.O1CCOCC1>[CH3:5][C:3]([CH2:2][CH:1]=[CH:1][CH:2]=[C:3]([CH3:5])[CH3:4])=[CH2:4]

Participants

6

Procedure

50 ml of distilled isoprene, 1 kg of dioxane, 5 g (16.5 mmol) of palladium acetylacetonate, 23.1 g (82.5 mmol) of tricyclohexylphosphine and 1.9 g (16.5 mmol) of 85% phosphoric acid in a four-necked flask are held under reflux under an argon atmosphere until the internal temperature exceeds 90°C. 1 kg of isoprene is then added dropwise at an oil-bath temperature of 120°C in such a manner that the internal temperature does not fall below 88°C (ca 30 ml/hour) but remains in the range of 90°-95°C. After 50 hours, the isoprene addition is terminated, the product now consisting essentially of 2,7-dimethyl-1,3,7-octatriene. The mixture is left to react for a further 40 hours, the internal temperature rising to 105°-108°C. The dioxane is now removed on a rotary evaporator at 40°C/20 mm Hg. The black-coloured residual oil is steam-distilled, 780 g of distillate being obtained. The residue (trimers and polymers) amounts to 215 g. By fractional distillation of the oil on a Raschig-ring column at 63°C/10 mm Hg, there are obtained 550 g of 2,7-dimethyl-1,4,6-octatriene; nD20 =1.4885. Odour: fatty, green, soapy, terpene-like.

Workup

  1. temperatureunder reflux under an argon atmosphere until the internal temperature
  2. customexceeds 90°C
  3. customdoes not fall below 88°C
  4. customremains in the range of 90°-95°C
  5. customis terminated
  6. waitThe mixture is left
  7. customto react for a further 40 hours
  8. customrising to 105°-108°C
  9. customThe dioxane is now removed on a rotary evaporator at 40°C/20 mm Hg
  10. distillationThe black-coloured residual oil is steam-distilled
  11. custom780 g of distillate being obtained
  12. distillationBy fractional distillation of the oil on a Raschig-ring column at 63°C/10 mm Hg, there

Sources & evidence

ORD record
ord-ebf9ae94fd884717bd3188c202fdd980
Source dataset
uspto-grants-1976_07
Patent number
US03970592

Reaction notes

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