2-Nitrophenol → 4-Hydroxy-3-nitrobenzene-1-sulfonyl chloride
反応式
[Cl:1][S:2]([OH:5])(=O)=[O:3].[N+:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[OH:15])([O-:8])=[O:7]>>[OH:15][C:10]1[CH:11]=[CH:12][C:13]([S:2]([Cl:1])(=[O:5])=[O:3])=[CH:14][C:9]=1[N+:6]([O-:8])=[O:7]参加物
3
反応条件
- 温度
- 60 °C
実験手順
To a solution of chlorosulfonic acid (12.0 mL, 180 mmol) at 0° C. was added 2-nitrophenol (8.35 g, 60.0 mmol) in small portions over 1 h. The reaction was heated to 60° C. for 20 minutes and allowed to stir for 18 h at 25° C. The reaction was quenched by pouring it into 100 g of ice. The reaction was extracted with chloroform (3×), washed with cold water (2×), dried over MgSO4, filtered, and concentrated to give 9.06 g (64%) of the title compound.
後処理
- customThe reaction was quenched
- additionby pouring it into 100 g of ice
- extractionThe reaction was extracted with chloroform (3×)
- washwashed with cold water (2×)
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-87a57751c10b4acda31417e824a1f39b
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08193227B2
反応ノート
読み込み中…