1,1,1-Trifluoro-2-iodoethane → Methyl 3-[(2,2,2-trifluoroethyl)sulfanyl]benzoate
反応式
[CH3:1][O:2][C:3](=[O:11])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([SH:10])[CH:5]=1.[F:12][C:13]([F:17])([F:16])[CH2:14]I>>[CH3:1][O:2][C:3](=[O:11])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([S:10][CH2:14][C:13]([F:17])([F:16])[F:12])[CH:5]=1参加物
3
実験手順
3-(2,2,2-Trifluoroethylthio)benzoic acid methyl ester was prepared 3-mercaptobenzoic acid methyl ester and trifluoroethyl iodide by following Method C. The reaction was conducted at room temperature overnight. The crude residue was chromatographed in 10-20% EtOAc/hexanes to afford 3-(2,2,2-trifluoroethylthio)benzoic acid methyl ester (82% yield).
後処理
- customThe crude residue was chromatographed in 10-20% EtOAc/hexanes
出典と根拠
- ORDレコード
- ord-158d5743fcc84cc4883141f7e7f700e3
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07691843B2
反応ノート
読み込み中…