HRID840735

反应详情

EQUATION

反应方程式

HRID 840735 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

A −78° C. solution of the dioxolane of Example 23(a) in dry THF (93 mL, Aldrich) was treated with n-butyllithium (34 mL, 50.7 mmol, 1.49 M/hexanes, Aldrich). The mixture was stirred at −78° C. for 35 minutes and then BrCF2CF2Br (6.1 mL, 51.1 mmol, Aldrich) was added. After 10 minutes, the mixture was allowed to warm to 0° C. and after 30 minutes at 0° C., the mixture was allowed to warm to room temperature. The solution was partitioned between H2O and ether (100 mL each). The layers were separated and the aqueous layer extracted with ether (100 mL). The combined ether solution was washed with 1 M sodium thiosulfate solution (2×100 mL) and brine (100 mL) and then was dried (MgSO4), filtered and evaporated to leave 11.15 g of 2-(2-Bromo-thiophen-3-yl)-[1,3]dioxolane as a yellow oil that was used directly in the next step.

WORKUP

后处理

  1. waitAfter 10 minutes
  2. temperatureto warm to 0° C. and after 30 minutes at 0° C.
  3. temperatureto warm to room temperature
  4. customThe solution was partitioned between H2O and ether (100 mL each)
  5. customThe layers were separated
  6. extractionthe aqueous layer extracted with ether (100 mL)
  7. washThe combined ether solution was washed with 1 M sodium thiosulfate solution (2×100 mL) and brine (100 mL)
  8. dry with materialwas dried (MgSO4)
  9. filtrationfiltered
  10. customevaporated