Tetrabutylammonium Fluoride → HCID 57503375, compound
Reaction equation
[F-].C([N+](CCCC)(CCCC)CCCC)CCC.[Si]([O:26][CH2:27][C:28]1[CH:29]=[C:30]([CH:48]=[CH:49][C:50]=1[CH2:51][O:52][Si](C(C)(C)C)(C)C)[O:31][CH2:32][C:33]1[CH:34]=[C:35]([CH:39]([CH3:47])[CH2:40][CH2:41][CH2:42][C:43]([CH3:46])([OH:45])[CH3:44])[CH:36]=[CH:37][CH:38]=1)(C(C)(C)C)(C)C>C1COCC1>[OH:26][CH2:27][C:28]1[CH:29]=[C:30]([CH:48]=[CH:49][C:50]=1[CH2:51][OH:52])[O:31][CH2:32][C:33]1[CH:34]=[C:35]([CH:39]([CH3:47])[CH2:40][CH2:41][CH2:42][C:43]([CH3:44])([OH:45])[CH3:46])[CH:36]=[CH:37][CH:38]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a manner similar to Example 3(i), by reacting 1.25 ml of tetrabutylammonium fluoride with 250 mg (0.41 mmol) of 6-{3-[3,4-bis-(tert-butyldimethylsilanyloxymethyl)phenoxymethyl]phenyl}-2-methylheptan-2-ol in 7 ml of THF, after purification on a silica column (ethyl acetate 30-heptane 70), a colourless oil (m=130 mg; Y=85%) is obtained.
Workup
- customafter purification on a silica column (ethyl acetate 30-heptane 70)
- customa colourless oil (m=130 mg; Y=85%) is obtained
Sources & evidence
- ORD record
- ord-1b0999968aa14bd385c4b0a579998cce
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06689922B1
Reaction notes
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