تفاعل #95510

ord-d4221ef4e3074261a4eed3b243a596f9

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONA mixture of 1.55 ml
  2. 2
    أخرىthe organic layer is separated
  3. 3
    غسيلwashed with water
  4. 4
    أخرىdried
  5. 5
    تركيزrefrigerated and then concentrated to an oil
  6. 6
    أخرىgiving 8.3 g
  7. 7
    workup.DISSOLUTIONThis oil is dissolved in 30 ml
  8. 8
    workup.WAITto stand for 3 hours
  9. 9
    درجة الحرارةheated at 45°-50° C. for 3 hours, refrigerated overnight
  10. 10
    تركيزconcentrated to about 1/3 its original volume
  11. 11
    workup.ADDITIONAn equal volume of ether is added
  12. 12
    أخرىproducing a gum
  13. 13
    أخرىThe solvent is removed
  14. 14
    workup.ADDITIONof ammonium hydroxide are added
  15. 15
    أخرىThe solid is collected
  16. 16
    غسيلwashed with water
  17. 17
    أخرىdried
  18. 18
    workup.DISSOLUTIONdissolved in 25 ml
  19. 19
    ترشيحfiltered and to the filtrate
  20. 20
    workup.ADDITIONare added alcoholic hydrogen chloride and ether
  21. 21
    ترشيحAfter refrigeration, the solid is filtered
  22. 22
    غسيلwashed with ether
  23. 23
    ترشيحof ethanol and filtered
  24. 24
    workup.ADDITIONThe filtrate is treated with alcoholic hydrogen chloride
  25. 25
    درجة الحرارةcooled
  26. 26
    أخرىgiving 0.41 g

الإجراء التجريبي

A mixture of 1.55 ml. of methanesulfonyl chloride and 40 ml. of toluene is added over a period of one hour to a stirred mixture of 5.8 g. of 4'-chloro-3,4-(methylenedioxy)benzoin, 5.6 ml. of triethylamine and 20 ml. of toluene. The mixture is allowed to stand 4 hours, 50 ml. of water and more toluene are added, the organic layer is separated, washed with water, dried, refrigerated and then concentrated to an oil, giving 8.3 g. of the methanesulfonate ester. This oil is dissolved in 30 ml. of acetone and added to a stirred mixture of 1.95 g. of hexahydro-2H-1,3-diazepin-2-thione in 150 ml. of acetone. The mixture is allowed to stand for 3 hours, heated at 45°-50° C. for 3 hours, refrigerated overnight and concentrated to about 1/3 its original volume. An equal volume of ether is added producing a gum. The solvent is removed, 100 ml. of water and 2 ml. of ammonium hydroxide are added. The solid is collected, washed with water, dried and dissolved in 25 ml. of ethanol. This solution is refrigerated, then filtered and to the filtrate are added alcoholic hydrogen chloride and ether. After refrigeration, the solid is filtered, washed with ether, boiled with 25 ml. of ethanol and filtered. The filtrate is treated with alcoholic hydrogen chloride and cooled, giving 0.41 g. of the desired product, m.p. 184°-186° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04344954uspto-grants-1982_08