تفاعل #462968

ord-ab58c36359f744d482c8691be7927a76

معادلة التفاعل

[K+].[OH-]
potassium hydroxide
NS(=O)(=O)c1ccccc1O
2-hydroxybenzenesulfonamide
FC(F)=C(F)Cl
chlorotrifluoroethylene
NS(=O)(=O)c1ccccc1OC(F)(F)C(F)Cl
title compound
المردود 60.7%
NS(=O)(=O)c1ccccc1OC(F)(F)C(F)Cl
2-(2-Chloro-1,1,2-trifluoroethoxy)-benzenesulfonamide
المردود 60.7%

المذيبات

ظروف التفاعل

درجة الحرارة
30°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGAt 40° to 50° C. and while stirring
  2. 2
    أخرىwas gassed in over a period of 12 hours
  3. 3
    ترشيحThe precipitate was filtered off under such and
  4. 4
    غسيلwashed with acetone
  5. 5
    أخرىThe filtrate was evaporated down under reduced pressure
  6. 6
    workup.STIRRINGstirred into 700 ml of water, suction
  7. 7
    ترشيحfiltered
  8. 8
    غسيلwashed
  9. 9
    أخرىdried

الإجراء التجريبي

At 25 bis 30° C. and while stirring, 5.9 g (0.093 mol) of 88% strength potassium hydroxide powder was added over a period of 5 minutes to a solution of 28.4 g (0.164 Mol) of 2-hydroxybenzenesulfonamide in 200 ml of acetone. At 40° to 50° C. and while stirring, 29.6 g (0.254 mol) of chlorotrifluoroethylene was gassed in over a period of 12 hours. The precipitate was filtered off under such and washed with acetone. The filtrate was evaporated down under reduced pressure, stirred into 700 ml of water, suction filtered, washed and dried. There was obtained 28.8 g (60.7%) of the title compound of m.p. 113° to 116° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05488029uspto-grants-1996_01