반응 #2286306

ord-3b92b59bce5b45ca98dafd27a48aecf8

반응 방정식

CC(C)c1cc(Oc2c(Cl)cc(CCO)cc2Cl)nn(C)c1=O
6-[2,6-dichloro-4-(2-hydroxy-ethyl)-phenoxy]-4-isopropyl-2-methyl-pyridazin-3-one
CC(C)c1cc(Oc2c(Cl)cc(CCO)cc2Cl)nn(C)c1=O
6-[2,6-Dichloro-4-(2-hydroxyethyl)-phenoxy]-4-isopropyl-2-methyl-pyridazin-3-one
CC(C)=O.O=S(=O)(O)O.[O]=[Cr](=[O])=[O]
Jones Reagent
CC(C)c1cc(Oc2c(Cl)cc(CC(=O)O)cc2Cl)nn(C)c1=O
[3,5-dichloro-4-(5-isopropyl-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-acetic acid
수율 19.0%
CC(C)c1cc(Oc2c(Cl)cc(CC(=O)O)cc2Cl)nn(C)c1=O
[3,5-Dichloro-4-(5-isopropyl-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-acetic acid
수율 19.0%

용매

반응 조건

온도
11°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축The reaction mixture was then concentrated under vacuum
  2. 2
    workup.ADDITIONThe resulting residue was diluted with ethyl acetate (25 mL) and water (20 mL)
  3. 3
    workup.ADDITIONwas treated with sodium bisulfite (100 mg)
  4. 4
    workup.STIRRINGThe resulting mixture was shaken
  5. 5
    기타The aqueous layer was separated
  6. 6
    추출was re-extracted with ethyl acetate (25 mL)
  7. 7
    세척washed with a saturated aqueous sodium chloride solution
  8. 8
    기타The organic layer was separated
  9. 9
    건조dried with sodium sulfate
  10. 10
    여과filtered
  11. 11
    농축concentrated under vacuum
  12. 12
    기타The resulting solid was recrystallized from ethyl acetate
  13. 13
    기타dried under vacuum overnight

실험 절차

A solution of 6-[2,6-dichloro-4-(2-hydroxy-ethyl)-phenoxy]-4-isopropyl-2-methyl-pyridazin-3-one (36) (330 mg, 0.92 mmol) in acetone (5 mL) was treated with Jones Reagent (0.51 mL of a 2.7M solution) slowly dropwise at 10° C. The resulting red reaction mixture was stirred at 11° C. for 30 min. The reaction mixture was then concentrated under vacuum. The resulting residue was diluted with ethyl acetate (25 mL) and water (20 mL) and was treated with sodium bisulfite (100 mg). The resulting mixture was shaken and turned from red to green. The aqueous layer was separated and was re-extracted with ethyl acetate (25 mL). The organic layers were combined and washed with a saturated aqueous sodium chloride solution. The organic layer was separated, dried with sodium sulfate, filtered, and concentrated under vacuum. The resulting solid was recrystallized from ethyl acetate and dried under vacuum overnight to afford [3,5-dichloro-4-(5-isopropyl-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-acetic acid (37) (70 mg, 19%) as a white solid; EI(+)-HRMS) m/z calcd for C16H16Cl2N2O4 (M+H)+ 371.0560, found 371.0561. Molecular Weight=371.2229; Exact Mass=370.0487

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE046024E1uspto-grants-2016_06