반응 #347145

ord-04919f6c8d2544c5adf2e90f16b6d4f1

반응 방정식

Cl
hydrochloric acid
[Na+].[OH-]
sodium hydroxide
CCCCCCCCN(CCCCCCCC)CCCCCCCC
trioctylamine
C[O-].[Na+]
sodium methoxide
O=C1OC(=O)c2c(F)c(F)c(F)c(F)c21
tetrafluorophthalic anhydride
COc1c(F)c(F)cc(C(=O)O)c1F
3-methoxy-2,4,5-trifluorobenzoic acid
수율 81.5%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Into a 100 ml glass reactor equipped with a reflux condenser and a stirrer
  2. 2
    온도under reflux
  3. 3
    온도After cooling
  4. 4
    온도Then, under reflux
  5. 5
    workup.STIRRINGthe mixture was stirred for one hour
  6. 6
    workup.STIRRINGthe mixture was stirred for 12 hors
  7. 7
    온도under reflux
  8. 8
    온도After cooling
  9. 9
    workup.STIRRINGthe mixture was stirred
  10. 10
    기타The organic layer was separated
  11. 11
    workup.STIRRINGstirred at 140° C. for 2 hours
  12. 12
    기타After completion of the reaction, 30 ml of a 20% sodium hydroxide aqueous solution
  13. 13
    workup.ADDITIONwas added
  14. 14
    workup.STIRRINGstirred
  15. 15
    기타The aqueous phase was separated
  16. 16
    추출extracted with ethyl acetate
  17. 17
    workup.DISTILLATIONThe solvent was distilled off

실험 절차

Into a 100 ml glass reactor equipped with a reflux condenser and a stirrer, 10 g (0.0397 mol) of the tetrafluorophthalic anhydride prepared in Example 3 and 20 ml of methanol were charged, and the mixture was stirred for 2 hours under reflux. After cooling, 42.8 g (0.079 mol) of a 10% methanol solution of sodium methoxide was dropwise added thereto. Then, under reflux, the mixture was stirred for one hour. Then, 15.9 g of a 10% sodium hydroxide aqueous solution was added thereto and the mixture was stirred for 12 hors under reflux. After cooling, 8 g of a 20% hydrochloric acid aqueous solution was added. Further, 21.1 g (0.0596 mol) of trioctylamine and 40 g of xylene were added thereto, and the mixture was stirred. The organic layer was separated and stirred at 140° C. for 2 hours. After completion of the reaction, 30 ml of a 20% sodium hydroxide aqueous solution was added thereto and stirred. The aqueous phase was separated and neutralized with a 10% hydrochloric acid aqueous solution and extracted with ethyl acetate. The solvent was distilled off to obtain 6.7 g of 3-methoxy-2,4,5-trifluorobenzoic acid. The yield was 81.5%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05523476uspto-grants-1996_06