反应 #2032

ord-6cc52ce6268b484891e547260b4cddbc

反应方程式

[K+].[OH-]
KOH
CCC#CCO
2-pentyn-1-ol
Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonyl chloride
CCC#CCOS(=O)(=O)c1ccc(C)cc1
2-pentyn-1-yl p-toluenesulphonate
收率 76.4%
CCC#CCOS(=O)(=O)c1ccc(C)cc1
2-pentyn-1-yl p-toluenesulfonate
收率 76.4%

溶剂

反应条件

温度
-10°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他to exceed -5° C
  2. 2
    萃取the product extracted into CH2Cl2

实验过程

A solution of 2-pentyn-1-ol (8.40 g, 100 mmol) in THF (60 mL) was treated with p-toluenesulfonyl chloride (23.9 g, 125 mmol) at -10° C., followed by pulverized KOH (11.3 g, 200 mmol) without allowing the temperature to exceed -5° C. After 1.5 hours of stirring at -10° C., 50 mL of saturated brine was added and the product extracted into CH2Cl2. The product, 2-pentyn-1-yl p-toluenesulphonate (2), was isolated by flash chromatography (18.17 g 76.4% yield). 1H NMR (200 MHz) δ: 7.81 (d, J=8.4 Hz, 2H, arom. CH), 7.33 (d, J=7.9 Hz, 2H, arom. CH), 4.68 (t, J=2.2, 2.2 Hz, 2H, CH2O-1), 2.44 (s, 3H, arom. CH3), 2.13 (tq, J=2.2, 2.2, 2.2, 7.5, 7.5 Hz, 2H, CH2 -4), 1.00 (t, J=7.5, 7.5 Hz, 3H, CH3 -5).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05728376uspto-grants-1998_03