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Butyl Acrylate → HCID 68185504, Verbindung

HRID 2095389
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2095389
[C:1]([O:5][CH2:6][CH2:7][CH2:8][CH3:9])(=[O:4])[CH:2]=[CH2:3].[CH:10]([Si:13]([CH:22]([CH3:24])[CH3:23])([CH:19]([CH3:21])[CH3:20])[N:14]1[CH:18]=[CH:17][CH:16]=[CH:15]1)([CH3:12])[CH3:11].C(OOC(C)(C)C)(=O)C1C=CC=CC=1>C(O)(=O)C.O1CCOCC1.CS(C)=O.C(OCC)C.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH:22]([Si:13]([CH:10]([CH3:12])[CH3:11])([CH:19]([CH3:21])[CH3:20])[N:14]1[CH:18]=[CH:17][C:16](/[CH:3]=[CH:2]/[C:1]([O:5][CH2:6][CH2:7][CH2:8][CH3:9])=[O:4])=[CH:15]1)([CH3:24])[CH3:23]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 3

HCID 8846Butyl AcrylateHCID 11966tert-Butyl peroxybenzoateHCID 145136N-Triisopropylsilylpyrrole

Produkt 1

HCID 68185504HCID 68185504, VerbindungAusbeute 133,5 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 167845palladium(II) acetateKatalysator
HCID 962
Water
Lösungsmittel
HCID 3283Diethyl EtherLösungsmittel
HCID 86642677HCID 86642677, VerbindungLösungsmittel

Reaktionsbedingungen

Temperatur
35 °C

Versuchsvorschrift

Palladium(II) acetate (0.05 equiv.) was added to a solution of n-butyl acrylate (0.27 mL, 1.5 mmol, 0.50 equiv.), 1-(triisopropylsilyl)-1H-pyrrole (1.34 g, 3.00 mmol), and tert-butyl peroxybenzoate (0.56 mL, 1.5 mmol, 0.50 equiv.), in acetic acid/dioxane/dimethylsulfoxide (0.23/0.69/0.08 mL). The mixture was stirred at 35° C. for 24 h, diluted with diethyl ether (200 mL) and water (20 mL), and filtered through a plug of celite. The organic phase was separated and washed with saturated NaHCO3 solution (2×30 mL) and water (30 mL). The combined aqueous layers were further extracted with CH2Cl2. The combined organic extracts were dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by CC (SiO2, EtOAc/petroleum ether 1:20) to give (E)-butyl 3-[1-(triisopropylsilyl)-1H-pyrrol-3-yl]acrylate (0.70 g, 67%) as a light-yellow oil.

Aufarbeitung

  1. filtrationfiltered through a plug of celite
  2. customThe organic phase was separated
  3. washwashed with saturated NaHCO3 solution (2×30 mL) and water (30 mL)
  4. extractionThe combined aqueous layers were further extracted with CH2Cl2
  5. dry with materialThe combined organic extracts were dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by CC (SiO2, EtOAc/petroleum ether 1:20)

Quellen und Nachweise

ORD-Eintrag
ord-97472cde517343538cc8de56267ca16b
Quelldatensatz
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08445684B2

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