반응 #1797490

ord-2cf66b25d21d4c67abab6115ac9eb043

반응 방정식

O=[N+]([O-])[O-].O=[N+]([O-])[O-].O=[N+]([O-])[O-].[Nd+3]
neodymium nitrate
CCN(CC)CC
triethylamine
CCN(CC)CC
triethylamine
O=[N+]([O-])[O-].O=[N+]([O-])[O-].O=[N+]([O-])[O-].[Nd+3]
neodymium nitrate
COc1ccccc1C(=O)O
2-methoxybenzoic acid
[Nd]
neodymium
COc1ccccc1C(=O)O
2-methoxybenzoic acid
수율 85.0%

반응 조건

온도
25°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Specifically, a reactor similar to that of 1-1 was used
  2. 2
    workup.STIRRINGto stir a slurry solution
  3. 3
    기타obtained
  4. 4
    온도by cooling in an ice water bath
  5. 5
    온도the solution was heated for 30 minutes at 40° C.
  6. 6
    workup.STIRRINGNext, while stirring this synthesis solution
  7. 7
    기타holding at 25° C.
  8. 8
    기타a solution obtained
  9. 9
    온도the solution was heated to 40° C.
  10. 10
    온도the clouding increased with time
  11. 11
    workup.WAITAfter another 20 minutes
  12. 12
    workup.ADDITIONwere further added
  13. 13
    workup.STIRRINGthe solution was stirred for another hour at 40° C.
  14. 14
    온도cooled
  15. 15
    기타the reaction
  16. 16
    기타Next, crystals obtained
  17. 17
    여과by filtering this slurry solution
  18. 18
    workup.ADDITIONwere added to 200 ml of methanol
  19. 19
    workup.STIRRINGstirred
  20. 20
    세척washed
  21. 21
    workup.ADDITION200 ml of methanol were once again added to the crystals
  22. 22
    workup.STIRRINGstirred
  23. 23
    세척washed
  24. 24
    여과filtered
  25. 25
    기타The resulting crystals were dried under reduced pressure at 50° C.

실험 절차

The compound was synthesized by the same method as that for Synthesis Example 1-2 above, that is, after forming a triethylamine salt of 2-methoxybenzoic acid in anhydrous ethanol, an ethanol solution of neodymium nitrate was added while stirring. Specifically, a reactor similar to that of 1-1 was used to stir a slurry solution obtained by adding 100 ml of an anhydrous ethanol to 45.65 g (0.3 mol) of 2-methoxybenzoic acid, while dripping 30.4 g (0.3 mol) of triethylamine while maintaining at 20-30° C. by cooling in an ice water bath. After dripping about one-third of the triethylamine, the slurry disappeared and became transparent. After dripping, the solution was heated for 30 minutes at 40° C. to prepare a transparent synthesis solution of 2-methoxybenzoic acid-triethylamine salts. Next, while stirring this synthesis solution and holding at 25° C., a solution obtained by dissolving 43.8 g of neodymium nitrate into 120 ml of ethanol was dripped in. Upon completion of dripping, the solution was heated to 40° C., began to cloud after 40 minutes, and the clouding increased with time. After another 20 minutes, it became an extremely thick slurry solution, so 100 ml of ethanol were further added, and the solution was stirred for another hour at 40° C., then cooled to end the reaction. Next, crystals obtained by filtering this slurry solution were added to 200 ml of methanol, stirred and washed, then refiltered, and 200 ml of methanol were once again added to the crystals, stirred and washed, then filtered. The resulting crystals were dried under reduced pressure at 50° C., to obtain 50.83 g of a neodymium salt of 2-methoxybenzoic acid (yield 85%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07790290B2uspto-grants-2010_09