反応 #2286306
ord-3b92b59bce5b45ca98dafd27a48aecf8
反応方程式
反応物
試薬
溶媒
反応条件
後処理
- 1濃縮The 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
- 5その他The aqueous layer was separated
- 6抽出was re-extracted with ethyl acetate (25 mL)
- 7洗浄washed with a saturated aqueous sodium chloride solution
- 8その他The organic layer was separated
- 9乾燥dried with sodium sulfate
- 10ろ過filtered
- 11濃縮concentrated under vacuum
- 12その他The resulting solid was recrystallized from ethyl acetate
- 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