Tetrabutylammonium Fluoride → HCID 54295887, compound
Reaction equation
[NH2:1][C@@:2]1([N:24]2[CH2:32][C:30](CO[Si](C(C)(C)C)(C)C)([CH3:31])[C:28](=[O:29])[NH:27][C:25]2=[O:26])[O:16][C@H:6]([CH:7]([Si](C(C)(C)C)(C)C)[OH:8])[C@@:4]([Si](C(C)(C)C)(C)C)([OH:5])[CH2:3]1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1COCC1>[NH2:1][C@@:2]1([N:24]2[CH:32]=[C:30]([CH3:31])[C:28](=[O:29])[NH:27][C:25]2=[O:26])[O:16][C@H:6]([CH2:7][OH:8])[C@@H:4]([OH:5])[CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of 1'-amino-3',5'-bis(t-butyldimethylsilyl)-5-t-butyldimethylsiloxymethyl thymidine and tetrabutylammonium fluoride in THF stands at room temperature for one hour. The solvent is evaporated and the residue chromatographically separated on silica.
Workup
- customThe solvent is evaporated
- customthe residue chromatographically separated on silica
Sources & evidence
- ORD record
- ord-d613241ad10e4bc88d9b91cb0200bc62
- Source dataset
- uspto-grants-1997_10
- Patent number
- US05681940
Reaction notes
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