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Triphenylphosphine → 1-[(E)-3-bromo-1-methyl-1-propenyl]-3-nitrobenzene

HRID 1826402
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1826402
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Br:20]Br.[N+:22]([C:25]1[CH:26]=[C:27](/[C:31](/[CH3:35])=[CH:32]/[CH2:33]O)[CH:28]=[CH:29][CH:30]=1)([O-:24])=[O:23]>C(#N)C>[Br:20][CH2:33]/[CH:32]=[C:31](/[C:27]1[CH:28]=[CH:29][CH:30]=[C:25]([N+:22]([O-:24])=[O:23])[CH:26]=1)\[CH3:35]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 11776TriphenylphosphineHCID 24408BromineHCID 69554909(E)-3-(3-nitrophenyl)-2-buten-1-ol

Produkt 1

HCID 695548111-[(E)-3-bromo-1-methyl-1-propenyl]-3-nitrobenzene

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel3×

Versuchsvorschrift

To a solution of triphenylphosphine (5.15 g, 19.7 mmol) in acetonitrile (140 ml) was added dropwise over 5 minutes a solution of bromine (3.15 g, 19.7 mmol) in acetonitrile (5 ml) at a rate such that the temperature did not exceed −10° C. The mixture was allowed to warm to room temperature, then to this was added a solution of (E)-3-(3-nitrophenyl)-2-buten-1-ol (Preparation 2, 4 g, 20.7 mmol) in acetonitrile (5 ml). The mixture was warmed gently to 65° C. for 1 h, cooled to room temperature and then poured onto diethyl ether (50 ml). The mixture was concentrated in vacuo, then diethyl ether (200 ml) was added. The mixture was filtered, concentrated again in vacuo and the residue purified by silica column (300 g) chromatography, eluting with 3:1 hexane/dichloromethane then 1:1 hexane/dichloromethane. Appropriate fractions were combined and concentrated in vacuo to give the title compound as a very pale yellow oil (4 g, 75%).

Aufarbeitung

  1. customdid not exceed −10° C
  2. temperatureThe mixture was warmed gently to 65° C. for 1 h
  3. temperaturecooled to room temperature
  4. additionpoured onto diethyl ether (50 ml)
  5. concentrationThe mixture was concentrated in vacuo
  6. additiondiethyl ether (200 ml) was added
  7. filtrationThe mixture was filtered
  8. concentrationconcentrated again in vacuo
  9. customthe residue purified by silica column (300 g) chromatography
  10. washeluting with 3:1 hexane/dichloromethane
  11. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-09856ba663cd48cc9d2fd6f51612900e
Quelldatensatz
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07049444B2

Notizen zur Reaktion

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