3-Bromo-1-(trimethylsilyl)-1-propyne → HCID 13065300, compound
Reaction equation
[Br:1][C:2]1[C:10]([Br:11])=[C:9]2[C:5]([CH2:6][CH:7]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:8]2=[O:12])=[CH:4][C:3]=1[O:19][CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22].Br[CH2:27][C:28]#[C:29][Si:30]([CH3:33])([CH3:32])[CH3:31]>>[Br:1][C:2]1[C:10]([Br:11])=[C:9]2[C:5]([CH2:6][C:7]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)([CH2:27][C:28]#[C:29][Si:30]([CH3:33])([CH3:32])[CH3:31])[C:8]2=[O:12])=[CH:4][C:3]=1[O:19][CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22]Participants
3
Procedure
Reaction of ethyl (6,7-dibromo-1-oxo-2-phenyl-5-indanyloxy)acetate with 1-bromo-3-(trimethylsilyl)-2propyne according to the procedure of Example 1, STEP (b), affords the title compound.
Sources & evidence
- ORD record
- ord-6923c64c530c4b10b09ed352a14885cb
- Source dataset
- uspto-grants-1982_06
- Patent number
- US04334088
Reaction notes
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