Reaktion #366916

ord-518a0ec7647f4a57965d7c05cbb3d5cb

Reaktionsgleichung

NS(=O)(=O)c1ccccc1Oc1ccccc1
2-phenoxyphenylsulfonamide
CCCCCCN=C=O
n-hexyl isocyanate
C1CN2CCN1CC2
1,4-diazabicyclo-[2,2,2]-octane
O=C(Cl)OC(Cl)(Cl)Cl
trichloromethyl chloroformate
O=C=NS(=O)(=O)c1ccccc1Oc1ccccc1
2-phenoxyphenylsulfonylisocyanate
Ausbeute 82.6%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAt the end of the reaction
  2. 2
    workup.DISTILLATIONthe xylene and n-hexyl isocyanate were distilled off

Vorschrift

25.0 g of 2-phenoxyphenylsulfonamide, 14.0 g of n-hexyl isocyanate, a catalytic amount of 1,4-diazabicyclo-[2,2,2]-octane and 150 ml xylene were refluxed with stirring for an hour. Thereafter, the mixture was reacted with a solution of 11.9 g of trichloromethyl chloroformate in 30 ml of xylene in a manner similar to that of Example (1). At the end of the reaction, the xylene and n-hexyl isocyanate were distilled off, to obtain 22.8 g of 2-phenoxyphenylsulfonylisocyanate. B.p. 146°-150° C./0.7 mmHg.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04586951uspto-grants-1986_05