Perfluoropropyl iodide → HCID 178448065, compound
Reaction equation
[CH2:1]([C@H:4]1[CH2:9][CH2:8][C@H:7]([CH:10]2[CH2:15][CH2:14][CH:13]=[CH:12][CH2:11]2)[CH2:6][CH2:5]1)[CH2:2][CH3:3].[F:16][C:17]([F:26])([C:22]([F:25])([F:24])[F:23])[C:18](I)([F:20])[F:19]>[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CCCCCC>[CH2:1]([C@H:4]1[CH2:9][CH2:8][C@H:7]([C@H:10]2[CH2:15][CH2:14][C@H:13]([C:18]([F:20])([F:19])[C:17]([F:26])([F:16])[C:22]([F:25])([F:24])[F:23])[CH2:12][CH2:11]2)[CH2:6][CH2:5]1)[CH2:2][CH3:3]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 0.1 mol of 4-(trans-4-propylcyclohexyl)-cyclohex-1-ene, 0.1 mol of heptafluoropropyl iodide, 10 mol % of tetrakis-(triphenylphosphine)-palladium and 200 ml of hexane is heated under reflux for 24 hours (compare T. Ishihara, Chemistry Letters (1986) 1895). The isomer mixture of the addition product thus formed is, after the catalyst has been filtered off, first heated with tributyl-tin hydride for 90 hours in toluene and reduced. The all-trans product>.trans-4-(trans-4-propylcyclohexyl)-1-heptafluoropropylcyclohexane, is finally obtained by separating the thiourea inclusion compound from a solution in methanol.
Workup
- temperatureis heated
- temperatureunder reflux for 24 hours (compare T. Ishihara, Chemistry Letters (1986) 1895)
- additionThe isomer mixture of the addition product
- customthus formed
- filtrationafter the catalyst has been filtered off
- temperaturefirst heated with tributyl-tin hydride for 90 hours in toluene
Sources & evidence
- ORD record
- ord-eebc84b8072b4261b919be9dc41d8084
- Source dataset
- uspto-grants-1994_09
- Patent number
- US05348677
Reaction notes
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