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Toluene → HCID 54102009, Verbindung

HRID 573494
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 573494
[PH4+].[C:2]1([CH3:8])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:9](=[O:12])([O-])[O-:10].[K+].[K+].[CH:15](=O)/[CH:16]=C/C>O>[C:9]([O:10][CH2:15][CH3:16])(=[O:12])[CH2:3][CH2:4][CH:5]=[CH:6][CH:7]=[CH:2][CH3:8]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 1140TolueneHCID 11430Potassium CarbonateHCID 447466CrotonaldehydeHCID 5460504Phosphonium

Produkt 1

HCID 54102009HCID 54102009, VerbindungAusbeute 74 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

Next, in a stream of nitrogen, the phosphonium salt (b) (420 g, 0.92 mol), toluene (1600 ml), potassium carbonate (506.2 g, 3.66 mol), and crotonaldehyde (256.7 g, 3.66 mol) were put into a 5-L flask, followed by stirring at 65° C. for 7 hours. The reaction solution was cooled to room temperature, and water (840 g) was put thereinto, followed by stirring for 30 minutes, and then subjected to separation of liquid. The solvent was evaporated from the organic layer under a reduced pressure. A solid thus precipitated was removed by filtration. This solution was distilled under a reduced pressure (65 to 70° C./1.5 torr), and ethyl 4,6-octadienoate (c) was obtained (114.4 g, yield 74%).

Aufarbeitung

  1. temperatureThe reaction solution was cooled to room temperature
  2. stirringby stirring for 30 minutes
  3. customsubjected to separation of liquid
  4. customThe solvent was evaporated from the organic layer under a reduced pressure
  5. customA solid thus precipitated
  6. customwas removed by filtration
  7. distillationThis solution was distilled under a reduced pressure (65 to 70° C./1.5 torr)

Quellen und Nachweise

ORD-Eintrag
ord-d2309b1d195b4e4ea8b719d5727d0844
Quelldatensatz
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09029593B2

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