Ethylamine → HCID 54456877, compound
Reaction equation
[CH3:1][C:2](=[CH:6][CH2:7][CH2:8][C:9]([CH3:31])=[CH:10][CH2:11][CH2:12][C:13]([CH3:30])=[CH:14][CH2:15][CH2:16][C:17]([CH3:29])=[CH:18][CH2:19][CH2:20][C:21]([CH3:28])=[CH:22][CH2:23][CH2:24][C:25](=[O:27])[CH3:26])[C:3](O)=O.[CH2:32]([NH2:34])[CH3:33].[C:35](OC(=O)C)(=[O:37])[CH3:36]>>[CH2:32]([N:34]([CH2:3][C:2]([CH3:1])=[CH:6][CH2:7][CH2:8][C:9]([CH3:31])=[CH:10][CH2:11][CH2:12][C:13]([CH3:30])=[CH:14][CH2:15][CH2:16][C:17]([CH3:29])=[CH:18][CH2:19][CH2:20][C:21]([CH3:28])=[CH:22][CH2:23][CH2:24][C:25](=[O:27])[CH3:26])[C:35](=[O:37])[CH3:36])[CH3:33]Participants
4
Procedure
Starting materials: 2,6,10,14,18-pentamethyl-22-oxo-2,6,10,14,18-tricosapentaenoic acid; ethylamine (70% aqueous ethylamine solution); and acetic anhydride.
Sources & evidence
- ORD record
- ord-f2ad0dc84b774810b8d4259f6f51fdcf
- Source dataset
- uspto-grants-1989_12
- Patent number
- US04888439
Reaction notes
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