تفاعل #63602

ord-9a978e6b54644696a6d3ec32141b02be

معادلة التفاعل

c1ccsc1
thiophene
CCO
ethanol
Cc1cc([N+](=O)[O-])ccc1NC(=O)CCl
2-chloro-N-(2-methyl-4-nitrophenyl)acetamide
[H][H]
hydrogen
Cc1cc(N)ccc1NC(=O)CCl
N-(4-amino-2-methylphenyl)-2-chloroacetamide
المردود 92.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthe catalyst was filtered off
  2. 2
    أخرىthe filtrate was evaporated
  3. 3
    أخرىThe solid residue was purified by column-chromatography over silica gel using
  4. 4
    workup.ADDITIONa mixture of trichloromethane and methanol (95:5 by volume) as eluent
  5. 5
    أخرىThe pure fractions were collected
  6. 6
    أخرىthe eluent was evaporated
  7. 7
    ترشيحThe product was filtered off
  8. 8
    أخرىdried

الإجراء التجريبي

To 1 part of a solution of 2 parts of thiophene in 40 parts of ethanol were added 15 parts of 2-chloro-N-(2-methyl-4-nitrophenyl)acetamide and 400 parts of methanol. The whole was hydrogenated at normal pressure and at room temperature with 2 parts of platinum-on-charcoal catalyst 5%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The solid residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was suspended in 2,2'-oxybispropane. The product was filtered off and dried, yielding 12 parts (92%)of N-(4-amino-2-methylphenyl)-2-chloroacetamide (intermediate 70).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04766125uspto-grants-1988_08