Isoprene → HCID 15664015, compound
Reaction equation
[C:1]1([CH3:9])[C:2]([NH2:8])=[CH:3][CH:4]=[CH:5][C:6]=1[NH2:7].[CH2:10]=[CH:11][C:12](=[CH2:14])[CH3:13].CCCCC>>[CH3:13][C:12]([CH3:14])=[CH:11][CH2:10][C:3]1[CH:4]=[CH:5][C:6]([NH2:7])=[C:1]([CH3:9])[C:2]=1[NH2:8]Participants
4
Procedure
A 200 g (1.64 mol) portion of 2,6-toluenediamine, 167 g (2.45 mol) of isoprene, 200 g (2.78 mol) of pentane, and 20 g of powdered H-Y zeolite were reacted at 150° C. in a similar fashion as indicated in Example 1. Isolation of a catalyst free sample was obtained by hot filtration. Selective removal of all residual hydrocarbon by vacuum distillation afforded the following product mixture:
Workup
- customIsolation of a catalyst free sample was obtained by hot filtration
- customremoval of all residual hydrocarbon
- distillationby vacuum distillation
- customafforded the following product mixture
Sources & evidence
- ORD record
- ord-5993220217a14d739cca3fb1fd7066e5
- Source dataset
- uspto-grants-1991_01
- Patent number
- US04985159
Reaction notes
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