Penta-1,3-diene → HCID 557558, compound
Reaction equation
[CH2:1]=[CH:2][CH:3]=[CH:4][CH3:5].[H][H]>>[CH3:1][C:3]1[CH2:4][CH2:5][CH:2]=[CH:3][CH2:4][CH2:1][C:2]=1[CH3:5]Participants
Procedure
20 Ml (100 mmoles) of 50 percent piperylene in other C5 hydrocarbons, 10 ml of toluene, 0.19 g (0.5 mmole) of tris(2,4-pentanedionato-O,O')-iron (also known as iron tri(acetylacetonate), CA registry number [14024-18-1]) and 0.3 g (1.0 mmole) of N,N'-(1,2-dimethyl-1,2-ethanediylidene)bis[4-methoxy-benzenamine] (CA registry [19215-52-2]) are combined under nitrogen in a 50-ml three-necked flask equipped with reflux condenser and nitrogen inlet. The mixture is stirred magnetically and heated to 55° C. 1.5 ml of triisobutyl aluminum (1.0M in toluene--1.5 mmoles) is added. A sample is taken after 1.6 hours and analyzed by gas chromatography. Piperylene is 90 percent converted. The dimethyl cyclooctadiene yield is 71 percent based on converted piperylene. In this embodiment R is methyl, R' is hydrogen and y is 2.
Sources & evidence
- ORD record
- ord-5c91bed2b77c4b4a9acbbec7671bcda3
- Source dataset
- uspto-grants-1984_07
- Patent number
- US04458061
Reaction notes
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