4-Bromobiphenyl → 4-BROMO-4'-SULFOBIPHENYL
反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.Cl[S:15]([OH:18])(=[O:17])=[O:16]>C(Cl)(Cl)Cl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([S:15]([OH:18])(=[O:17])=[O:16])=[CH:10][CH:9]=2)=[CH:6][CH:7]=1参加物
4
実験手順
A 500 mL round-bottom-flask equipped with an addition funnel, stirring bar, and gas inlet was charged with 4-bromo-biphenyl (50 g, 0.215 mol) and chloroform (200 mL) then purged with nitrogen. Chlorosulfonic acid (18 mL, 0.27 mol) was added dropwise to the solution from the addition funnel then stirred for 1 hour. The resulting precipitate was collected by vacuum filtration, washed with cold chloroform, and dried under vacuum to give 61.97 g of 4′-bromo-biphenyl-4-sulfonic acid (92% yield).
後処理
- customA 500 mL round-bottom-flask equipped with an addition funnel
- customthen purged with nitrogen
- stirringthen stirred for 1 hour
- filtrationThe resulting precipitate was collected by vacuum filtration
- washwashed with cold chloroform
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-8e8a19e18e314e7689fa1daf4f9bae08
- 出典データセット
- uspto-grants-2011_03
- 特許番号
- US07910653B2
反応ノート
読み込み中…