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Isopropanol → Methyl 5-bromo-2-oxopentanoate

HRID 1906858
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1906858
CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O.[Br:14][CH2:15][CH2:16][CH2:17][CH:18]([OH:23])[C:19]([O:21][CH3:22])=[O:20].C(O)(C)C>CC(C)=O.O>[Br:14][CH2:15][CH2:16][CH2:17][C:18](=[O:23])[C:19]([O:21][CH3:22])=[O:20]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 3776IsopropanolHCID 13769948Methyl 5-bromo-2-hydroxypentanoateHCID 131709961Jones' reagent

Produkt 1

HCID 13769949Methyl 5-bromo-2-oxopentanoateAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 180AcetoneLösungsmittelHCID 962
Water
Lösungsmittel

Versuchsvorschrift

Jones' reagent (CrO3 : 9.58 g, H2SO4 : 8.47 ml, H2O: 36.8 ml) was added to a magnetically stirred solution of Part (3) compound (12.53 g, 59.3 mmole) in acetone (150 ml) at room temperature. The addition was controlled to maintain the temperature below 35° C. After the completion of the addition, the reaction was stirred at room temperature for 45 minutes. Isopropyl alcohol (30 ml) was added dropwise and stirred for 30 minutes. The reaction was then diluted with H2O (500 ml) and the products were extracted with CH2Cl2 (1 l.). The CH2Cl2 layer was washed with brine (100 ml×3) and dried over MgSO4. Filtration and evaporation of solvents gave the title compound (11.4 g, 54.5 mmole, 92%) as a colorless liquid.

Aufarbeitung

  1. additionThe addition
  2. temperatureto maintain the temperature below 35° C
  3. additionAfter the completion of the addition
  4. stirringstirred for 30 minutes
  5. extractionthe products were extracted with CH2Cl2 (1 l.)
  6. washThe CH2Cl2 layer was washed with brine (100 ml×3)
  7. dry with materialdried over MgSO4
  8. filtrationFiltration and evaporation of solvents

Quellen und Nachweise

ORD-Eintrag
ord-4e2cd350fe7c4d4b8bde57090990c9c2
Quelldatensatz
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04654357

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