Pyrrolidine → HCID 54423824, compound
Reaction equation
[CH3:1][C:2](=[CH:6][CH2:7][CH2:8][C:9]([CH3:26])=[CH:10][CH2:11][CH2:12][C:13]([CH3:25])=[CH:14][CH2:15][CH2:16][C:17]([CH3:24])=[CH:18][CH2:19][CH2:20][C:21](=[O:23])[CH3:22])[C:3]([OH:5])=O.[NH:27]1[CH2:31][CH2:30][CH2:29][CH2:28]1>>[CH3:1][C:2](=[CH:6][CH2:7][CH2:8][C:9]([CH3:26])=[CH:10][CH2:11][CH2:12][C:13]([CH3:25])=[CH:14][CH2:15][CH2:16][C:17]([CH3:24])=[CH:18][CH2:19][CH2:20][C:21](=[O:23])[CH3:22])[C:3]([N:27]1[CH2:31][CH2:30][CH2:29][CH2:28]1)=[O:5]Participants
3
Procedure
Starting materials: 2,6,10,14-tetramethyl-18-oxo-2,6,10,14-nonadecatetraenoic acid and pyrrolidine.
Sources & evidence
- ORD record
- ord-d1be2437afab4d46bce02ae9834fec13
- Source dataset
- uspto-grants-1989_12
- Patent number
- US04888439
Reaction notes
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