Tetrabutylammonium Fluoride → HCID 44815235, compound
Reaction equation
[CH3:1][C:2]1([C:11]#[C:12][Si](C)(C)C)[CH2:7][CH2:6][C:5](=[O:8])[C:4]([C:9]#[N:10])=[CH:3]1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1COCC1.C(Cl)Cl.CCOCC>[C:11]([C:2]1([CH3:1])[CH2:7][CH2:6][C:5](=[O:8])[C:4]([C:9]#[N:10])=[CH:3]1)#[CH:12]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 10 (20 mg, 0.086 mmol) in THF (0.6 mL) was degassed by gentle argon stream for 5 min. To the solution was added tetra-(n-butyl)ammonium fluoride (TBAF, 70 mg). The mixture was stirred at room temperature for 20 min. The mixture was diluted with methylene chloride/ether (1:2, 20 mL). The mixture was extracted with saturated aqueous sodium bicarbonate solution (10 mL×3). The basic extract was acidified with 5% aqueous HCl solution. The acidic mixture was extracted with methylene chloride/ether (1:2, 10 mL×4). The extract was washed with water (10 mL×2), dried over MgSO4, and filtered. The filtrate was evaporated in vacuo to give a crystalline solid. The solid was purified by preparative TLC [hexanes-ethyl acetate (2.5:1)] to give MCE-3 as a crystalline solid (6.9 mg, 50%): 1H NMR (CDCl3) δ 7.39 (1H, d, J=1.8 Hz), 2.84 (1H, m), 2.62 (1H, m), 2.38 (1H, s), 2.32 (1H, m), 2.05 (1H, m), 1.55 (3H, s).
Workup
- extractionThe mixture was extracted with saturated aqueous sodium bicarbonate solution (10 mL×3)
- extractionThe basic extract
- extractionThe acidic mixture was extracted with methylene chloride/ether (1:2, 10 mL×4)
- washThe extract was washed with water (10 mL×2)
- dry with materialdried over MgSO4
- filtrationfiltered
- customThe filtrate was evaporated in vacuo
- customto give a crystalline solid
- customThe solid was purified by preparative TLC [hexanes-ethyl acetate (2.5:1)]
Sources & evidence
- ORD record
- ord-7b2eba00ad7048bba0a42ac537ae2db2
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08314137B2
Reaction notes
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