Stannane, tributyl(1-ethoxyethenyl)- → HCID 118557861, compound
Reaction equation
Br[C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH2:8][CH:9]1[CH2:17][C:16]2[C:11](=[CH:12][CH:13]=[C:14]([CH3:18])[CH:15]=2)[C:10]1=[O:19].[CH2:20]([O:22]C([Sn](CCCC)(CCCC)CCCC)=C)[CH3:21]>>[C:20]([C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH2:8][CH:9]1[CH2:17][C:16]2[C:11](=[CH:12][CH:13]=[C:14]([CH3:18])[CH:15]=2)[C:10]1=[O:19])(=[O:22])[CH3:21]Participants
3
Procedure
The title compound 114 is prepared according to the procedure reported in Example 36.5 with compound 105 (750 mg, 2.38 mmol) and (1-ethoxyvinyl)tri(n-butyl)stannane (0.8 mL, 238 mmol) as reactants. White solid. (Yield 398.8 mg, 60%).
Sources & evidence
- ORD record
- ord-0cc17b792155459abaf659354c6ffb15
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09376387B2
Reaction notes
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