反应 #718227

ord-1ee24bbd5ce349fcb3189db0ffea2bea

反应方程式

CCCCCCCCCCCCc1ccccc1
1-phenyldodecane
O=S(=O)(O)O
H2SO4
[K+].[OH-]
KOH
CCCCCCCCCCCCc1ccc(S(=O)(=O)[O-])cc1.[K+]
potassium 4-dodecylbenzene sulfonate
收率 84.0%

试剂

反应条件

温度
90°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度cooled to room temperature
  2. 2
    workup.ADDITIONgradually poured
  3. 3
    过滤The resulting white precipitate was collected by filtration
  4. 4
    洗涤washed with cold water (40 mL)
  5. 5
    其他dried

实验过程

A mixture of 1-phenyldodecane (7.5 g, 30.5 mmol) and concentrated H2SO4 (8.4 mL) was stirred vigorously at 90° C. for 1 h, cooled to room temperature, and then gradually poured with stirring into 10% aqueous KOH solution (175 mL). The resulting white precipitate was collected by filtration, washed with cold water (40 mL) and dried to give potassium 4-dodecylbenzene sulfonate (10.6 g, 29.1 mmol, 84%). This salt (10.0 g, 27.5 mmol) and POCl3 (4.2 g, 27.4 mmol) were stirred at room temperature and gradually heated to 170° C. The hot reaction mixture was poured into cold water and extracted with CHCl2. The organic layer was washed with water, dried over anhydrous Na2SO4, and filtered. Evaporation of the volatiles yielded p-dodecylbenzenesulfonyl chloride as a pale yellow liquid (9.2 g, 97%) which eventually became crystalline, mp 33° C.; 1H NMR (300 MHz, CDCl3) δ 0.88 (t, 3H, J=6.5), 1.20-1.38 (m, 18H), 1.60-1.68 (m, 2H), 2.72 (t, 2H, J=7.5 Hz), 7.40 (d, 2H, J=8.4 Hz), 7.79 (d, 2H, J=8.4 Hz); 13C NMR (75 MHz, CDCl3) δ 14.1, 22.6, 29.1, 29.3, 29.3, 29.5, 29.6, 30.9, 31.9, 36.0, 127.0, 129.6, 141.7, 151.6.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09320734B2uspto-grants-2016_04