Ethanol → Ethyl 2-(2-chloro-6-iodophenyl)acetate
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([I:8])[C:3]=1[CH2:9][C:10]([OH:12])=[O:11].OS(O)(=O)=O.[CH3:18][CH2:19]O>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([I:8])[C:3]=1[CH2:9][C:10]([O:12][CH2:18][CH3:19])=[O:11]参加物
4
実験手順
A mixture of 2-(2-chloro-6-iodophenyl)acetic acid (10 g, 34 mmol) in 100 mL EtOH was treated with 2 mL concentrated H2SO4, and refluxed for 15 hours. The resulting mixture was cooled to room temperature and concentrated. The residue was diluted with 200 mL EtOAc, washed with water (3×50 mL), saturated NaCl (20 mL), dried over sodium sulfate and concentrated. The crude mixture was purified by column chromatography (10-20% EtOAc/hexane) to give 9.5 g of pale yellow oil. MS m/e: (M+H)+ 324.
後処理
- temperaturerefluxed for 15 hours
- concentrationconcentrated
- additionThe residue was diluted with 200 mL EtOAc
- washwashed with water (3×50 mL), saturated NaCl (20 mL)
- dry with materialdried over sodium sulfate
- concentrationconcentrated
- customThe crude mixture was purified by column chromatography (10-20% EtOAc/hexane)
出典と根拠
- ORDレコード
- ord-e991e78fcad645968a76ea268da8ca92
- 出典データセット
- uspto-grants-2009_12
- 特許番号
- US07635715B2
反応ノート
読み込み中…