Trimethylsilylacetylene → HCID 18953340, compound
Reaction equation
[CH3:1][C:2]([CH3:25])([CH3:24])[CH2:3][C:4]12[CH2:11][O:10][C:7]([C:12]3[CH:17]=[CH:16][C:15]([C:18]#[C:19][Si](C)(C)C)=[CH:14][CH:13]=3)([O:8][CH2:9]1)[O:6][CH2:5]2.CC(C)(C)CC12CO[C:32](C3C=CC(I)=CC=3)(OC1)[O:31][CH2:30]2.C[Si](C#C)(C)C>>[CH3:1][C:2]([CH3:25])([CH3:24])[CH2:3][C:4]12[CH2:11][O:10][C:7]([C:12]3[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][CH2:30][O:31][CH3:32])=[CH:14][CH:13]=3)([O:8][CH2:9]1)[O:6][CH2:5]2Participants
4
Procedure
Using methodology described in Example 1, 4-(2,2-dimethylpropyl)-1-[4-(2-trimethylsilylethynyl)phenyl]-2,6,7-trioxabicyclo[2,2,2]octane was prepared from 4-(2,2-dimethyl-propyl)-1-(4-iodophenyl)-2,6,7-trioxabicyclo[2,2,2]octane and trimethylsilylacetylene.
Sources & evidence
- ORD record
- ord-a51338cd8142492da4ff189b64035888
- Source dataset
- uspto-grants-1994_12
- Patent number
- US05371075
Reaction notes
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