反応 #2286306

ord-3b92b59bce5b45ca98dafd27a48aecf8

反応方程式

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
収率 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
収率 19.0%

溶媒

反応条件

温度
11°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    濃縮The 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
    その他The aqueous layer was separated
  6. 6
    抽出was re-extracted with ethyl acetate (25 mL)
  7. 7
    洗浄washed with a saturated aqueous sodium chloride solution
  8. 8
    その他The organic layer was separated
  9. 9
    乾燥dried with sodium sulfate
  10. 10
    ろ過filtered
  11. 11
    濃縮concentrated under vacuum
  12. 12
    その他The resulting solid was recrystallized from ethyl acetate
  13. 13
    その他dried under vacuum overnight

実験手順

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

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE046024E1uspto-grants-2016_06