تفاعل #74901

ord-52d400b817b54f0b9a95b00dd6f2ed59

معادلة التفاعل

[O-][N+](=S)c1cccc(C(F)(F)CF)c1Cl
2-chloro 1,1,2-trifluoroethylthio nitrobenzene
O=[N+]([O-])c1cccc(S)c1
3-nitrothiophenol
[K+].[OH-]
potassium hydroxide
FC(F)=C(F)Cl
2-chloro-1,1,2-trifluoroethylene
O=[N+]([O-])c1cccc(SC(F)(F)C(F)Cl)c1
3(2-Chloro-1,1,2-trifluoroethylthio) nitrobenzene

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONA mixture of 50 g
  2. 2
    درجة الحرارةThe reaction mixture is cooled
  3. 3
    أخرىdecanted
  4. 4
    أخرىthe solution evaporated to dryness in vacuo
  5. 5
    workup.ADDITIONis added
  6. 6
    استخلاصthe product extracted with methylene chloride
  7. 7
    غسيلThe extracts are washed with 2.5 N aqueous sodium hydroxide and water
  8. 8
    أخرىdried
  9. 9
    أخرىevaporated to dryness in vacuo
  10. 10
    أخرىaffording 76.5 g

الإجراء التجريبي

A mixture of 50 g. (0.322 moles) of 3-nitrothiophenol, 46.6 g. (0.402 moles) of potassium hydroxide, 60 ml. of acetone and 59 g. (0.395 moles) of 2-chloro-1,1,2-trifluoroethylene is heated in an autoclave with stirring for 11/2 hours at 60°-70° C. The reaction mixture is cooled, decanted and the solution evaporated to dryness in vacuo. The oily residue is combined with the solids, water is added and the product extracted with methylene chloride. The extracts are washed with 2.5 N aqueous sodium hydroxide and water, dried and evaporated to dryness in vacuo affording 76.5 g. of 3(2-chloro 1,1,2-trifluoroethylthio nitrobenzene with a b.p. at 0.25 mm. of mercury of 98°-102° C. The structure is verified with nuclear magnetic resonance.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04174400uspto-grants-1979_11