反应 #66017
ord-54b763fa48f0470b873aab1b94d435ed
反应方程式
sulphonic acid
4-phenoxybenzenesulphonic acid
thionyl chloride
→
4-Phenoxy-benzenesulphonyl chloride
溶剂
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1温度at reflux
- 2其他The solvent was evaporated
- 3workup.DISSOLUTIONthe residue dissolved in Et20 (40 mL)
- 4洗涤The ether solution was washed with 5% aqueous NaOH (3×40 mL) and water (6×40 mL)
- 5干燥dried over anhydrous MgSO4
- 6过滤filtered
- 7浓缩concentrated in vacuo
- 8其他After drying in high vacuum overnight
- 9其他the pure product was obtained as a white solid
实验过程
The sulphonic acid (2a) was dissolved in an excess of thionyl chloride (30 mL), a catalytic amount of DMF (cat) was added, and the resulting mixture was stirred for 6 h at reflux. The solvent was evaporated and the residue dissolved in Et20 (40 mL). The ether solution was washed with 5% aqueous NaOH (3×40 mL) and water (6×40 mL), dried over anhydrous MgSO4, filtered, and concentrated in vacuo. After drying in high vacuum overnight, the pure product was obtained as a white solid. Yield 63%: 2.09 g, 7.44 mmol, (light yellow syrup). 1H-NMR (CDCl3): δ 7.44 (d, 3J=9.1 Hz, 2H, ArH), 7.38 (d, 3J=9.1 Hz, 2H, ArH), 7.19 (t, 1H, ArH), 7.12 (d, 3J=9.1 Hz, 2H, ArH), 6.98 (d, 3J=9.1 Hz, 2H, ArH)