反応式
C([O:8][C:9]1[CH:13]=[C:12]([C:14]([F:17])([F:16])[F:15])[S:11][CH:10]=1)C1C=CC=CC=1.ClC(Cl)(Cl)Cl.I[Si](C)(C)C>O>[OH:8][C:9]1[CH:13]=[C:12]([C:14]([F:17])([F:16])[F:15])[S:11][CH:10]=1参加物
5
反応条件
- 温度
- 60 °C
実験手順
A mixture of 1G (7.75 g) and tetrachloromethane (50 ml) was treated with iodotrimethylsilane (12.30 ml) and heated to 60° C. for 12 hours. The reaction mixture was stirred at room temperature for 12 hours. Water (50 ml) was added and the resulting reaction mixture was extracted with dichloromethane three times. The combined organic phases were washed with water and dried. The crude reaction mixture was eluted through hexane (100 g/silica gel) to remove benzyliodide and then with diethyl ether. The etheral phases were concentrated and distilled in vacuo to give the product (3.33 g, 74%) having a boiling point of 65°-66° C. at 4 mm.
後処理
- customthe resulting reaction mixture
- extractionwas extracted with dichloromethane three times
- washThe combined organic phases were washed with water
- customdried
- customThe crude reaction mixture
- washwas eluted through hexane (100 g/silica gel)
- customto remove benzyliodide
- concentrationThe etheral phases were concentrated
- distillationdistilled in vacuo
出典と根拠
- ORDレコード
- ord-5390bef8f83d469c87d4be81a5a5a2b1
- 出典データセット
- uspto-grants-1999_02
- 特許番号
- US05869426
関連ノート
読み込み中…