Diallylamine → HCID 66662345, compound
Reaction equation
C(NCC=C)C=C.[CH2:8]([N:11](CC=C)[C:12]1[CH:17]=[CH:16][C:15]([C:18]2([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:20][CH2:19]2)=[CH:14][CH:13]=1)[CH:9]=[CH2:10]>>[CH2:8]([NH:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]2([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:19][CH2:20]2)=[CH:14][CH:13]=1)[CH:9]=[CH2:10]Participants
3
Procedure
This compound was prepared from the N-2-propenyl-2-propen-1-amine using the coupling protocol outlined in example 258, step 2. The other major product was tert-butyl 1-[4-(diallylamino)phenyl]cyclopropanecarboxylate.
Sources & evidence
- ORD record
- ord-8cb92a51a865455cb4d587bb1c3a56f5
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09126927B2
Reaction notes
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