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1-Phenyl-1,2-propanedione → 3-Bromo-1-phenylpropane-1,2-dione

HRID 236286
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 236286
[C:1]1([C:7](=[O:11])[C:8](=[O:10])[CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:12]Br>C(Cl)(Cl)Cl>[Br:12][CH2:9][C:8](=[O:10])[C:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)=[O:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 113631-Phenyl-1,2-propanedioneHCID 24408Bromine2×

Produkt 1

HCID 125689113-Bromo-1-phenylpropane-1,2-dioneAusbeute 102 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel2×

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

5.32 kg of 1-phenylpropane-1,2-dione (98.6% by G.C. equivalent to 5.24 kg, 35.4 mole) were dissolved in 36 liters of chloroform and the solution was heated to 50° C. A solution of 5.66 kg (35.4 mole) of bromine in 8 liters of chloroform was added slowly to maintain a gentle reflux and immediate decolorization of the bromine (approximately 6 hours). The solution was cooled to room temperature overnight and was washed with 20 liters of saturated sodium bicarbonate solution and 20 liters of water and dried over sodium sulfate. The solvent was removed under vacuum to obtain 8.2 kg (100% yield) of a green/yellow oil which was used directly for subsequent reactions after estimation of its purity (approximately 75% by G.C. or N.M.R.).

Aufarbeitung

  1. temperatureto maintain
  2. temperaturea gentle reflux
  3. temperatureThe solution was cooled to room temperature overnight
  4. washwas washed with 20 liters of saturated sodium bicarbonate solution and 20 liters of water
  5. dry with materialdried over sodium sulfate
  6. customThe solvent was removed under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-501fe104ed934cbc80f2252f8a7f9dfa
Quelldatensatz
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04643999

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