HRID1722236

反应详情

EQUATION

反应方程式

HRID 1722236 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-30 °C

PROCEDURE

实验过程

4-bromophenylacetylene (10 g, 55 mmol), prepared according to Organic Reactions 5 (1), 50, (1949), in dry dimethyl sulphoxide (70 ml) was added to lithium amide (from 66 mmol) of lithium) in liquid ammonia (200 ml). The mixture was stirred for 1 hour at -30° C., 2-(2-bromoethyl)-1,3-dioxolane (10 g, 55 mmol) was added and the mixture was stirred for 2 hours at -30° C. Ammonium chloride (12 g) was added, the ammonia was allowed to evaporate and water (200 ml) was added to the residue. The emulsion was extracted with ether and the organic phase was washed with brine and dried. The solvents were removed and the product purified by dry column chromatography (silica, 5% ether in hexane 1:1 ether:hexane) to give 4.08 g (26% of theory) of 5-(4'bromophenyl)-4-pentyn-1-al ethylene acetal.

WORKUP

后处理

  1. stirringthe mixture was stirred for 2 hours at -30° C
  2. customto evaporate
  3. additionwater (200 ml) was added to the residue
  4. extractionThe emulsion was extracted with ether
  5. washthe organic phase was washed with brine
  6. customdried
  7. customThe solvents were removed
  8. customthe product purified
  9. dry with materialby dry column chromatography (silica, 5% ether in hexane 1:1 ether:hexane)