Pyrrolidine → HCID 54430439, compound
Reaction equation
[CH2:1]([O:3][C:4]([CH:6]=[C:7]([CH3:21])[CH2:8][CH2:9][CH:10]=[C:11]([CH3:20])[CH2:12][CH2:13][CH:14]=[C:15]([CH3:19])[C:16]([OH:18])=O)=[O:5])[CH3:2].[NH:22]1[CH2:26][CH2:25][CH2:24][CH2:23]1>>[CH2:1]([O:3][C:4]([CH:6]=[C:7]([CH3:21])[CH2:8][CH2:9][CH:10]=[C:11]([CH3:20])[CH2:12][CH2:13][CH:14]=[C:15]([CH3:19])[C:16]([N:22]1[CH2:26][CH2:25][CH2:24][CH2:23]1)=[O:18])=[O:5])[CH3:2]Participants
3
Procedure
Starting materials: 11-ethoxycarbonyl-2,6,10-trimethyl-2,6,10-undecatrienoic acid and pyrrolidine.
Sources & evidence
- ORD record
- ord-1af481b0d2f3406aa7e1174f131625b6
- Source dataset
- uspto-grants-1989_12
- Patent number
- US04888439
Reaction notes
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