Reaktion #1355

ord-6f4401e734f84a7c9ca25250dd8869e3

Reaktionsgleichung

CCCC(Cc1ccccc1Br)C(=O)O
3-(2-bromophenyl)-2-propylpropionic acid
O=S(Cl)Cl
thionyl chloride
CCCC(Cc1ccccc1Br)C(=O)Cl
crude product
CCCC(Cc1ccccc1Br)C(=O)Cl
3-(bromophenyl)-2-n-propylpropionyl chloride

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA 500-ml three-necked round flask equipped with a stirring bar
  2. 2
    Temperaturthe mixture was heated
  3. 3
    Temperaturunder reflux for 2 hours
  4. 4
    SonstigeThen, the excess thionyl chloride was removed by a single distillation
  5. 5
    workup.DISTILLATIONthe distillation of the residue under reduced pressure

Vorschrift

A 500-ml three-necked round flask equipped with a stirring bar, a Dimroth condenser, a thermometer and a NaOH trap was charged with 277 mmol of 3-(2-bromophenyl)-2-propylpropionic acid and 200 ml of thionyl chloride, and the mixture was heated under reflux for 2 hours. Then, the excess thionyl chloride was removed by a single distillation, and the distillation of the residue under reduced pressure gave 77.4 g of a crude product having a boiling point of 130° to 135° C./1 mmHg as a pale brown transparent liquid. This acid chloride was used in the next reaction without further purification

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723640uspto-grants-1998_03