Isoprene → 1,4,6-Octatriene, 2,7-dimethyl-, (E)-
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
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
- temperatureunder reflux under an argon atmosphere until the internal temperature
- customexceeds 90°C
- customdoes not fall below 88°C
- customremains in the range of 90°-95°C
- customis terminated
- waitThe mixture is left
- customto react for a further 40 hours
- customrising to 105°-108°C
- customThe dioxane is now removed on a rotary evaporator at 40°C/20 mm Hg
- distillationThe black-coloured residual oil is steam-distilled
- custom780 g of distillate being obtained
- 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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