Diisobutylamine → N-(2,6,10-trimethyl-14-oxo-2,6,10-pentadecatrienoyl)diisobutylamine
Reaction equation
[CH3:1][C:2](=[CH:6][CH2:7][CH2:8][C:9]([CH3:21])=[CH:10][CH2:11][CH2:12][C:13]([CH3:20])=[CH:14][CH2:15][CH2:16][C:17](=[O:19])[CH3:18])[C:3]([OH:5])=O.[CH2:22]([NH:26][CH2:27][CH:28]([CH3:30])[CH3:29])[CH:23]([CH3:25])[CH3:24]>>[CH3:1][C:2](=[CH:6][CH2:7][CH2:8][C:9]([CH3:21])=[CH:10][CH2:11][CH2:12][C:13]([CH3:20])=[CH:14][CH2:15][CH2:16][C:17](=[O:19])[CH3:18])[C:3]([N:26]([CH2:27][CH:28]([CH3:30])[CH3:29])[CH2:22][CH:23]([CH3:25])[CH3:24])=[O:5]Participants
3
Procedure
Starting materials: 2,6,10-trimethyl-14-oxo-2,6,10-pentadecatrienoic acid and diisobutylamine.
Sources & evidence
- ORD record
- ord-43a08ea214d94087b0ad81d1e1ca0077
- Source dataset
- uspto-grants-1989_12
- Patent number
- US04888439
Reaction notes
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