Reaktion #1576495

ord-ca9642abf1f94eaca83a79f5b40c43cb

Reaktionsgleichung

CCC(Cc1ccccc1-c1ccccc1)C(=O)O
3-(2-biphenylyl)-2-ethylpropionic acid
O=S(Cl)Cl
thionyl chloride
CCC(Cc1ccccc1-c1ccccc1)C(=O)Cl
crude product
Ausbeute 106.3%
CCC(Cc1ccccc1-c1ccccc1)C(=O)Cl
3-(2-biphenylyl)-2-ethylpropionyl chloride
Ausbeute 106.3%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeTo a 100-ml three-necked round flask (equipped with stirrer chip, Dimroth condenser
  2. 2
    Temperaturwere refluxed for 2.5 hours
  3. 3
    Temperaturwith heating in a nitrogen atmosphere
  4. 4
    workup.DISTILLATIONthe unreacted thionyl chloride was distilled off under reduced pressure

Vorschrift

To a 100-ml three-necked round flask (equipped with stirrer chip, Dimroth condenser, thermometer and NaOH trap) were introduced 13.3 g (52.4 mmol) of the 3-(2-biphenylyl)-2-ethylpropionic acid and 25.9 ml (355 mmol) of thionyl chloride, and they were refluxed for 2.5 hours with heating in a nitrogen atmosphere. After the reaction was completed, the unreacted thionyl chloride was distilled off under reduced pressure to obtain 15.2 g of a crude product of yellow orange liquid. This acid chloride was used for the next reaction without further purification. The properties of the product thus obtained are described below.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05677408uspto-grants-1997_10