تفاعل #48024

ord-1911c6d38c2143cabee43681d994bac6

معادلة التفاعل

NC(=NO)c1cccc(C(F)(F)F)c1
m-trifluoromethyl-benzamidoxime
[K+].[OH-]
potassium hydroxide
ClCC1CO1
epichlorohydrine
N=C(NOCC1CO1)c1cccc(C(F)(F)F)c1
m-trifluoromethyl-N-(2,3-epoxypropoxy)-benzamidine

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىkept in a refrigerator overnight
  2. 2
    استخلاصthe mixture was extracted with ethyl acetate (4×250 ml)
  3. 3
    غسيلThe combined organic phases were washed with water
  4. 4
    أخرىdried
  5. 5
    workup.ADDITIONtreated with charcoal
  6. 6
    أخرىevaporated to dryness

الإجراء التجريبي

50 g (0.245 mol) of m-trifluoromethyl-benzamidoxime and 33.7 g (0.6 mol) of potassium hydroxide was dissolved in a mixture of dimethyl sulphoxide and 170 ml of water, and the mixture was cooled to 0° C. 48 ml (0.6 mol) of epichlorohydrine was added, and the reaction mixture was stirred at 0° C. for 5 hours, then kept in a refrigerator overnight. Next day 250 ml of water was added, and the mixture was extracted with ethyl acetate (4×250 ml). The combined organic phases were washed with water, dried, treated with charcoal and evaporated to dryness, to yield m-trifluoromethyl-N-(2,3-epoxypropoxy)-benzamidine, as a colorless oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745465B2uspto-grants-2010_06