反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.[I:10]N1C(=O)CCC1=O>CC(O)=O>[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][C:3]=1[I:10]参加物
4
実験手順
To a stirred solution of 4-hydroxybenzaldehyde (2.0 g, 16.39 mmol) in AcOH (30 mL) was added N-iodosuccinimide (4.5 g, 19.67 mmol). The reaction mixture was stirred at r.t. for 16 h, then filtered. The filtrate was poured onto water (100 mL) and EtOAc (50 mL) was added. The aqueous fraction was separated, then extracted with EtOAc (3×50 mL). The combined organic fractions were washed with water (2×20 mL), dried (Na2SO4), filtered and concentrated in vacuo to give the title compound (2.0 g, 50%) as a white solid that was used without further purification. LCMS (ES−) 247.1 (M−H)−, RT 1.44 minutes (Method 9).
後処理
- filtrationfiltered
- additionThe filtrate was poured onto water (100 mL) and EtOAc (50 mL)
- additionwas added
- customThe aqueous fraction was separated
- extractionextracted with EtOAc (3×50 mL)
- washThe combined organic fractions were washed with water (2×20 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-9903c20f1b284e53b3d49920fa6a7c01
- 出典データセット
- uspto-grants-2012_12
- 特許番号
- US08338592B2
関連ノート
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