Pivaloyl chloride → HCID 178495557, Verbindung
Reaktionsgleichung
[Li+].C[Si]([N-][Si](C)(C)C)(C)C.[CH3:11][O:12][CH:13]=[CH:14][C:15](=[O:17])[CH3:16].[C:18](Cl)(=[O:23])[C:19]([CH3:22])([CH3:21])[CH3:20]>C1COCC1>[OH:23][C:18]([C:19]([CH3:22])([CH3:21])[CH3:20])=[CH:16][C:15](=[O:17])[CH:14]=[CH:13][O:12][CH3:11]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- -78 °C
Versuchsvorschrift
LiHMDS (1M in THF, 100 mL, 2 eq) is added dropwise to a cold (−78° C.) solution of 4-methoxy-3-buten-2-one (10 mL, 100 mmol, 2 eq) in THF (400 mL). After a 30 min stirring at −78° C., a solution of pivaloyl chloride (6.12 mL, 50 mmol) in THF (100 mL) is added. The resulting mixture is allowed to warm to it over 2 h and quenched by addition of a saturated solution of NH4Cl. THF is removed under vacuum. The concentrated mixture is extracted with Et2O. The organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. The residue is purified by silica gel column chromatography (Hex/EtOAc, 1:0→85:15) to afford 6.83 g of the title compound as a yellow oil: ESI-MS: 185.1 [M+H]+; TLC: Rf=0.87 (Hex/EtOAc, 1:1).
Aufarbeitung
- temperatureto warm to it over 2 h
- customquenched by addition of a saturated solution of NH4Cl
- customTHF is removed under vacuum
- extractionThe concentrated mixture is extracted with Et2O
- washThe organic phase is washed with brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customThe residue is purified by silica gel column chromatography (Hex/EtOAc, 1:0→85:15)
Quellen und Nachweise
- ORD-Eintrag
- ord-03bd81bf270943d89ed795a835a549dd
- Quelldatensatz
- uspto-grants-2012_07
- Patentnummer
- US08227462B2
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