Tetrabutylammonium Fluoride → HCID 86719094, compound
Reaction equation
[Si]([O:8][C:9]1[CH:10]=[CH:11][C:12]([CH2:15][C:16]([O:18][CH3:19])=[O:17])=[N:13][CH:14]=1)(C(C)(C)C)(C)C.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1>[OH:8][C:9]1[CH:10]=[CH:11][C:12]([CH2:15][C:16]([O:18][CH3:19])=[O:17])=[N:13][CH:14]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To the stirred solution of methyl 2-(5-((tert-butyldimethylsilyl)oxy)pyridin-2-yl)acetate (1 g, 3.5 mmol) in THF was added TBAF (1M, 3.5 ml) at room temperature. The whole mixture was stirred at room temperature overnight. It was evaporated and extracted with EtOAc, the organic layer was washed with water, evaporated and purified by a standard method.
Workup
- customIt was evaporated
- extractionextracted with EtOAc
- washthe organic layer was washed with water
- customevaporated
- custompurified by a standard method
Sources & evidence
- ORD record
- ord-e7dc8af142ad479495eb07675e6897f6
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09029531B2
Reaction notes
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