反応式
[I:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=[O:10])=[CH:4][CH:3]=1.OS(O)(=O)=O.[CH2:17](O)[CH3:18]>>[CH2:17]([O:10][C:9](=[O:11])[CH2:8][C:5]1[CH:4]=[CH:3][C:2]([I:1])=[CH:7][CH:6]=1)[CH3:18]参加物
4
実験手順
4-Iodophenylacetic acid (3 g), ethanol (20 mL) and conc. H2SO4 (5 mL) were refluxed overnight. Ca. 15 mL ethanol was then evaporated, the residue was extracted with dichloromethane (3×100 mL), the combined organic extracts were washed with sat. aq. NaHCO3, dried over Na2SO4 and evaporated in vacuo to afford 2.97 g (90%) of 121JP58 as a yellow oil.
後処理
- custom15 mL ethanol was then evaporated
- extractionthe residue was extracted with dichloromethane (3×100 mL)
- washthe combined organic extracts were washed with sat. aq. NaHCO3
- dry with materialdried over Na2SO4
- customevaporated in vacuo
出典と根拠
- ORDレコード
- ord-cb397d3af94241c2a8071375f0fb4a7e
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07538222B2
関連ノート
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