HRID1034165

反应详情

EQUATION

反应方程式

HRID 1034165 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

To a 5 liter 4-neck round-bottom flask fitted with mechanical stirrer, thermowell and addition funnel, under a nitrogen atmosphere, was added 78.4 ml of oxalyl chloride and 925 ml of dichloromethane. The reaction was cooled to -78° C. with a dry ice/acetone bath. Then 125.3 ml of distilled dimethylsulfoxide was added dropwise, maintaining the reaction temperature below -65° C. After the addition was complete, 138.4 g of 2-[(4-chlorobutyl)thio]benzyl alcohol was added in 300 ml of dichloromethane. After addition was complete, the mixture was stirred for 30 min., then 417.3 ml of triethylamine was added. The bath was allowed to warm gradually to room temperature and stirred overnight at this temperature. The reaction mixture was poured into a 12 liter flask containing a stirring mixture of 3100 g of crushed ice and 4730 ml of 1N HCl. After stirring for 30 min., the mixture was extracted with dichloromethane (3×300 ml) the organic solution was dried over magnesium sulfate, filtered and concentrated to a brown oil. The product was further purified by column chromatography on silica gel, eluting with 10% ethyl acetate in hexane to give 117.7 g of the pure product as an oil. 1H-NMR (CDCl3) δ 1.8-2.0(m,4H); 3.0(t,2H); 3.6(t,2H); 7.2-7.6(m,3H); 7.8(m,1H); 10.4(s,1H).

WORKUP

后处理

  1. customTo a 5 liter 4-neck round-bottom flask fitted with mechanical stirrer
  2. additionthermowell and addition funnel
  3. temperaturemaintaining the reaction temperature below -65° C
  4. additionAfter the addition
  5. additionAfter addition
  6. temperatureto warm gradually to room temperature
  7. stirringstirred overnight at this temperature
  8. additionThe reaction mixture was poured into a 12 liter flask
  9. additioncontaining
  10. stirringAfter stirring for 30 min.
  11. extractionthe mixture was extracted with dichloromethane (3×300 ml) the organic solution
  12. dry with materialwas dried over magnesium sulfate
  13. filtrationfiltered
  14. concentrationconcentrated to a brown oil
  15. customThe product was further purified by column chromatography on silica gel
  16. washeluting with 10% ethyl acetate in hexane