反応式
[Br:1][C:2]1[CH:3]=[C:4](C)[C:5](O)=[C:6]([CH:10]=1)[C:7](O)=O.[C:13]([O-:16])([O-])=[O:14].[K+].[K+].[CH3:19]I.[C:21]([O-:24])([O-])=O.[Cs+].[Cs+]>CC(C)=O.CN(C=O)C.O>[Br:1][C:2]1[CH:10]=[C:6]([CH3:7])[C:5]([O:24][CH3:21])=[C:4]([CH:3]=1)[C:13]([O:16][CH3:19])=[O:14]参加物
反応条件
- 温度
- 58 °C
実験手順
To a solution of 5-bromo-2-hydroxy-3-methyl-benzoic acid (3 g, 12.9 mmol, 1.0 eq) and K2CO3 (5.38 g, 38.9 mmol, 3.0 eq) in acetone (15 mL) was added MeI (5.53 g, 38.9 mmol, 3.0 eq). The mixture was stirred at 58° C. overnight. TLC indicated that the reaction was not completed. Water was added and the aqueous layer extracted with EtOAc. The organic extract was washed with water and brine, dried (Na2SO4) filtered and evaporated in vacuo. The crude solid obtained was dissolved in DMF (20 mL) and Cs2CO3 (6 g, 18.4 mmol, 1.4 eq) added. To the mixture was added MeI (2 mL, 38.95 mmol, 3 eq). The mixture was stirred for 1 h at room temperature, water was added and the aqueous layer was extracted with EtOAc. The combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and evaporated in vacuo to give the title compound as a white solid (2.6 g, 77%).
後処理
- extractionthe aqueous layer extracted with EtOAc
- extractionThe organic extract
- washwas washed with water and brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- customevaporated in vacuo
- customThe crude solid obtained
- stirringThe mixture was stirred for 1 h at room temperature
- extractionthe aqueous layer was extracted with EtOAc
- washThe combined organic extracts were washed with water and brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- customevaporated in vacuo
出典と根拠
- ORDレコード
- ord-a137cbb6b8e94faca9e92d005cb5808b
- 出典データセット
- uspto-grants-2016_02
- 特許番号
- US09249085B2
関連ノート
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