Toluene → 2-(Chloromethyl)-4-phenylthiophene
反応式
[C:1]1([C:7]2[CH:8]=[C:9]([CH2:12]O)[S:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1(C)C=CC=CC=1.S(Cl)([Cl:23])=O>N1C=CC=CC=1>[Cl:23][CH2:12][C:9]1[S:10][CH:11]=[C:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH:8]=1参加物
5
実験手順
4-Phenyl thiophene-2-methanol (0.21 g), toluene (2.0 mL), and a catalytic amount of pyridine were added, and thionyl chloride (0.16 mL) was added dropwise thereto under ice-cooling. After stirring at room temperature for 3 hours, the reaction mixture was concentrated under reduced pressure, azeotroped with toluene, and dried at 60° C. under reduced pressure to obtain 2-(chloromethyl)-4-phenylthiophene (0.22 g).
後処理
- temperatureunder ice-cooling
- concentrationthe reaction mixture was concentrated under reduced pressure
- customazeotroped with toluene
- customdried at 60° C. under reduced pressure
出典と根拠
- ORDレコード
- ord-4e3358ab301a4978a0f11c11dcb5fe3c
- 出典データセット
- uspto-grants-2013_12
- 特許番号
- US08598355B2
反応ノート
読み込み中…