Pyrrolidine → 1-((Z)-3-tributylstannanylallyl)pyrrolidine
Reaction equation
[CH2:1]([N:3]([CH2:20][CH3:21])[CH2:4]/[CH:5]=[CH:6]\[Sn:7]([CH2:16][CH2:17][CH2:18][CH3:19])([CH2:12][CH2:13][CH2:14][CH3:15])[CH2:8][CH2:9][CH2:10][CH3:11])[CH3:2].BrC/C=C\[Sn](CCCC)(CCCC)CCCC.N1CCCC1>>[CH2:8]([Sn:7]([CH2:16][CH2:17][CH2:18][CH3:19])([CH2:12][CH2:13][CH2:14][CH3:15])/[CH:6]=[CH:5]\[CH2:4][N:3]1[CH2:1][CH2:2][CH2:21][CH2:20]1)[CH2:9][CH2:10][CH3:11]Participants
4
Procedure
Prepared by proceeding in a similar manner to Intermediate 3, starting from ((Z)-3-bromoprop-1-enyl)tributylstannane (Intermediate 2) and pyrrolidine.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-95e0152e83544195963f6bcc2e8d7094
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09266896B2
Reaction notes
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