反应 #4002

ord-bd220c185fdc4f29a50c93efa6db59de

反应条件

温度
140°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.DISSOLUTIONThe solid dissolved
  2. 2
    温度The oil bath temperature was raised to 160° C.
  3. 3
    温度heating
  4. 4
    其他The heat was removed
  5. 5
    温度until cool
  6. 6
    workup.STIRRINGThe solid was stirred with 250 parts of ethyl acetate
  7. 7
    过滤filtered
  8. 8
    workup.DISSOLUTIONthe solid dissolved in 1000 parts of hot water
  9. 9
    workup.ADDITIONtreated with charcoal
  10. 10
    过滤filtered
  11. 11
    温度The aqueous solution was cooled
  12. 12
    workup.ADDITIONneutralised by the addition of saturated sodium acetate solution
  13. 13
    过滤The precipitated solid was filtered
  14. 14
    洗涤washed with water
  15. 15
    workup.DISSOLUTIONThis crude product was then dissolved in 550 parts of concentrated hydrochloric acid
  16. 16
    workup.ADDITIONdiluted with 800 parts of water
  17. 17
    workup.STIRRINGstirred with 5 parts of charcoal for 20 minutes
  18. 18
    过滤The solution was filtered
  19. 19
    其他the product precipitated by the addition of saturated sodium acetate solution to pH 6
  20. 20
    过滤The solid was filtered
  21. 21
    洗涤washed with water
  22. 22
    其他dried in a vacuum oven at 110° C.

实验过程

119 Parts of 4-chloro-4-(2,2,2-trichloroethyl)-oxetan-2-one and 95.5 parts of guanidine hydrochloride were charged to a reaction flask and heated in an oil bath at 140° C. for 15 minutes. The solid dissolved and HCl gas was evolved. The oil bath temperature was raised to 160° C. and heating was continued for a further 45 minutes. The heat was removed and the reaction mass was stirred until cool and solidified. The solid was stirred with 250 parts of ethyl acetate and filtered. The filtrate was discarded and the solid dissolved in 1000 parts of hot water, treated with charcoal and filtered. The aqueous solution was cooled and neutralised by the addition of saturated sodium acetate solution. The precipitated solid was filtered and washed with water. This crude product was then dissolved in 550 parts of concentrated hydrochloric acid, diluted with 800 parts of water and stirred with 5 parts of charcoal for 20 minutes. The solution was filtered and the product precipitated by the addition of saturated sodium acetate solution to pH 6. The solid was filtered, washed with water and dried in a vacuum oven at 110° C. to give 2-amino-4-(2,2-dichloro-vinyl)-6-hydroxypyrimidine m.p. 245°-248° C. (decomposition).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04723006uspto-grants-1988_02