Reaktion #459688

ord-600ed36075834fe29a03f0acf0741c75

Reaktionsgleichung

CCCC[C](C)(C)[Mg][Cl]
1,1-dimethylpentylmagnesium chloride
[Mg]
magnesium
CCCCC(C)(C)Cl
1-chloro-1,1-dimethylpentane
O=C(Cl)CCCCl
4-chloro-butyryl chloride
Cl
hydrochloric acid
CCCCC(C)(C)C(=O)CCCCl
product
CCCCC(C)(C)C(=O)CCCCl
1-Chloro-5,5-dimethyl-4-nonanone

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONis added dropwise
  2. 2
    SonstigeThe ether layer is separated
  3. 3
    Waschenwashed with water and brine
  4. 4
    Trocknendried over sodium sulfate
  5. 5
    SonstigeThe ether is evaporated
  6. 6
    workup.DISTILLATIONthe residue distilled at aspirator vacuum through a Vigreaux column

Vorschrift

Four hundred ml. of a solution in ether of 1,1-dimethylpentylmagnesium chloride prepared from magnesium (24.3 g., 1.0 mole) and 1-chloro-1,1-dimethylpentane (134.5 g., 1.0 mole) according to the procedure of Whitmore and Badertscher [J. Am. Chem. Soc., 55, 1559 (1933)] is added dropwise with stirring to 4-chloro-butyryl chloride (197 g., 1.4 moles) in ether (400 ml.) during 6 hours. The reaction mixture is stirred for an additional 12 hours. It is then poured into a mixture of ice and dilute hydrochloric acid. The ether layer is separated, washed with water and brine and dried over sodium sulfate. The ether is evaporated and the residue distilled at aspirator vacuum through a Vigreaux column to yield the product as a colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04091107uspto-grants-1978_05