Tetrabutylammonium Fluoride → 1-Decyn-3-ol
Reaktionsgleichung
C[Si](C)(C)[C:3]#[C:4][CH:5]([OH:13])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[CH:3]#[C:4][CH:5]([OH:13])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Dissolve 1-trimethylsilyl-1-decyn-3-ol (2.07 g, 9.13 mmol) in tetrahydrofuran (11 mL) and place under an argon atmosphere. Add, by dropwise addition, tetra-n-butylammonium fluoride (11 mL of a 1M solution in tetrahydrofuran, 11 mmol). Stir for 1 hour at room temperature and partition between methylene chloride and water. Separate the organic phase, wash with saturated aqueous sodium chloride, dry (MgSO4), filter and evaporate the solvent in vacuo to give the title compound.
Aufarbeitung
- custompartition between methylene chloride and water
- customSeparate the organic phase
- washwash with saturated aqueous sodium chloride
- dry with materialdry (MgSO4)
- filtrationfilter
- customevaporate the solvent in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-d93a649a9ef541aab87e984dfaebfa16
- Quelldatensatz
- uspto-grants-1992_10
- Patentnummer
- US05157167
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