반응 #1990603

ord-8c328956ae354663bed3f71eb97b569f

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출the whole mixture is extracted with ether
  2. 2
    workup.DISTILLATIONAfter distilling of the solvent
  3. 3
    workup.DISSOLUTIONthe residue is dissolved in methanol
  4. 4
    workup.ADDITION4.6 ml of a 30% sodium hydroxide solution is added
  5. 5
    workup.STIRRINGthe mixture is stirred at 60° C. for an hour
  6. 6
    세척The reaction mixture is washed with ether
  7. 7
    추출extracted with ethyl acetate
  8. 8
    세척The extract is washed with water
  9. 9
    기타dried
  10. 10
    workup.DISTILLATIONthe solvent distilled off
  11. 11
    기타the residue chromatographed on silica gel
  12. 12
    기타The crystals recovered from the chloroform-ethanol (17:1) eluate
  13. 13
    기타are recrystallized from ether-hexane

실험 절차

Aluminum chloride (2.5 g) is added portionwise in a nitrogen atmosphere to a solution of 1 g of methyl 21-chloroformylheneicosanoate and 1.7 g of 3,4,5-trimethoxytoluene in 50 ml of nitrobenzene, and the resulting mixture is stirred at room temperature for 48 hours. To the reaction mixture are added water and diluted hydrochloric acid, and the whole mixture is extracted with ether. After distilling of the solvent, the residue is dissolved in methanol, 4.6 ml of a 30% sodium hydroxide solution is added, and the mixture is stirred at 60° C. for an hour. The reaction mixture is washed with ether, then made acidic with diluted hydrochloric acid and extracted with ethyl acetate. The extract is washed with water and dried, the solvent distilled off, and the residue chromatographed on silica gel. The crystals recovered from the chloroform-ethanol (17:1) eluate are recrystallized from ether-hexane to give colorless crystals of 21-(2-hydroxy-3,4-dimethoxy-6-methylbenzoyl)heneicosanoic acid. m.p. 103°-150° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04436753uspto-grants-1984_03