Tetrabutylammonium Fluoride → HCID 67278732, compound
Reaction equation
[Si]([O:8][CH2:9][C:10]1[CH:11]=[C:12]([CH:25]=[CH:26][C:27]2[CH:28]=[C:29]([CH2:33][CH2:34][CH2:35][CH2:36][C:37]([CH3:40])([OH:39])[CH3:38])[CH:30]=[CH:31][CH:32]=2)[CH:13]=[C:14]([CH2:16][O:17][Si](C(C)(C)C)(C)C)[CH:15]=1)(C(C)(C)C)(C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1COCC1>[OH:17][CH2:16][C:14]1[CH:13]=[C:12]([CH:25]=[CH:26][C:27]2[CH:28]=[C:29]([CH2:33][CH2:34][CH2:35][CH2:36][C:37]([CH3:40])([OH:39])[CH3:38])[CH:30]=[CH:31][CH:32]=2)[CH:11]=[C:10]([CH2:9][OH:8])[CH:15]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a manner similar to Example 3(i), by reacting 858 mg (1.47 mmol) of 6-(3-{2-[3,5-bis-(tert-butyldimethylsilanyloxymethyl)phenyl]vinyl}phenyl)-2-methylhexan-2-ol with 3.25 ml of tetrabutylammonium fluoride 1M/THF, after purification on a silica column (ethyl acetate), a white paste (m=460 mg; Y=88%) is obtained.
Workup
- customafter purification on a silica column (ethyl acetate)
- customa white paste (m=460 mg; Y=88%) is obtained
Sources & evidence
- ORD record
- ord-c17a463bfb1c41c9bcf935a3c494b40b
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06689922B1
Reaction notes
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