Benzoyl Peroxide → Diethyl [(1E)-3-bromoprop-1-en-1-yl]phosphonate

HRID 2051962Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2051962
[CH:1](/[P:4](=[O:11])([O:8][CH2:9][CH3:10])[O:5][CH2:6][CH3:7])=[CH:2]\[CH3:3].[Br:12]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[Br:12][CH2:3]/[CH:2]=[CH:1]/[P:4](=[O:11])([O:5][CH2:6][CH3:7])[O:8][CH2:9][CH3:10]

Komponenten

5

Edukt 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 5702572Diethyl (1E)-prop-1-en-1-ylphosphonate

Produkt 1

HCID 5702525Diethyl [(1E)-3-bromoprop-1-en-1-yl]phosphonateAusbeute 58,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 5943Carbon TetrachlorideLösungsmittel

Versuchsvorschrift

To a solution of diethyl trans-1-propenylphosphonate (32.04 g.) in carbon tetrachloride (320 ml.) were added N-bromosuccinimide (41.65 g.) and dibenzoylperoxide (2.8 g.). The reaction mixture was heated to reflux for 1.5 hours and stirred for 30 minutes under ice-cooling. Insoluble materials were removed off by filtration and the filtrate was concentrated under reduced pressure to give an oily residue (63.09 g.), which was subjected to a column chromatography on silicagel and eluted with chloroform. The eluates were evaporated to dryness under reduced pressure to give an oily diethyl 3-bromo-trans-1-propenylphosphonate (27.04 g.).

Aufarbeitung

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 1.5 hours
  3. temperaturecooling
  4. customInsoluble materials were removed off by filtration
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customto give an oily residue (63.09 g.), which
  7. washeluted with chloroform
  8. customThe eluates were evaporated to dryness under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-9363f1fddaf74e7e887f8ec6a2a96546
Quelldatensatz
uspto-grants-1980_01
Patentnummer
US04182758

Notizen zur Reaktion

Wird geladen…