Tetrabutylammonium Fluoride → HCID 62372909, compound
Reaction equation
CCCC[N+](CCCC)(CCCC)CCCC.[F-].[Si]([O:26][CH2:27][CH:28]1[CH2:32][CH2:31][N:30]([C:33](=[O:38])[C:34]([F:37])([F:36])[F:35])[CH2:29]1)(C(C)(C)C)(C)C>C1COCC1>[F:37][C:34]([F:35])([F:36])[C:33]([N:30]1[CH2:31][CH2:32][CH:28]([CH2:27][OH:26])[CH2:29]1)=[O:38]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
TBAF was added to a THF solution of 3-({[tert-butyl(dimethyl)silyl]oxy}methyl)-1-(trifluoroacetyl)pyrrolidine and stirred overnight at room temperature. Thereafter, its work-up and purification were carried out in the standard method to obtain [1-(trifluoroacetyl)pyrrolidin-3-yl]methanol. EP: 198.
Workup
- customThereafter, its work-up and purification
Sources & evidence
- ORD record
- ord-f1564a3a00924549bac36c8eb85e3fd5
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07585886B2
Reaction notes
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