반응 #2286306
ord-3b92b59bce5b45ca98dafd27a48aecf8
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후처리
- 1농축The reaction mixture was then concentrated under vacuum
- 2workup.ADDITIONThe resulting residue was diluted with ethyl acetate (25 mL) and water (20 mL)
- 3workup.ADDITIONwas treated with sodium bisulfite (100 mg)
- 4workup.STIRRINGThe resulting mixture was shaken
- 5기타The aqueous layer was separated
- 6추출was re-extracted with ethyl acetate (25 mL)
- 7세척washed with a saturated aqueous sodium chloride solution
- 8기타The organic layer was separated
- 9건조dried with sodium sulfate
- 10여과filtered
- 11농축concentrated under vacuum
- 12기타The resulting solid was recrystallized from ethyl acetate
- 13기타dried 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