Hydrogen Bromide → 1-[2-(4-Fluorophenylthio)-6-fluorophenyl]3-bromoprop-1-ene
反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([F:15])[C:10]=2[CH:16](O)[CH:17]=[CH2:18])=[CH:4][CH:3]=1.C(OCC)C.[BrH:25].O>CCCCCC>[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([F:15])[C:10]=2[CH:16]=[CH:17][CH2:18][Br:25])=[CH:4][CH:3]=1参加物
6
実験手順
1-(2-(4-fluorophenylthio)-6-fluorophenyl)prop-2-en-1-ol (2.29 g, 8.23 mmol) is dissolved in 10 ml of hexane and 10 ml of diethyl ether and cooled in an ice bath. Concentrated HBr acid (4.6 ml, 41.2 mmol) is then added dropwise and the reaction mixture is stirred vigorously for 5 hours at room temperature. The reaction mixture is then poured into water and extracted twice with diethyl ether. The extracts are washed with water and then brine and dried over MgSO4 to afford the subtitle compound.
後処理
- extractionextracted twice with diethyl ether
- washThe extracts are washed with water
- dry with materialbrine and dried over MgSO4
出典と根拠
- ORDレコード
- ord-51a5f4a8e8dc4914ada856c72ccb657d
- 出典データセット
- uspto-grants-1994_02
- 特許番号
- US05283361
反応ノート
読み込み中…