HRID2304259

反应详情

EQUATION

反应方程式

HRID 2304259 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 solution of 2.8 g of 4-(4-Bromo-phenoxy)-tetrahydropyran in 75 mL of dry tetrahydrofuran was added 7.5 mL of n-butyllithium (1.6 N in hexane) at −78° C. After stirring at −78° C. for 2 hours the reaction mixture was allowed to warm to −40° C. and a solution of 4.1 mL of sulfuryl chloride in 75 mL of dry hexane was added within 15 minutes. Stirring was continued for 1 hour at −30° C. and subsequently for another hour at 5° C. The mixture was poured on ice, extracted with diethyl ether and the ether extract washed with cold water and brine, dried (sodium sulfate), and concentrated. The residue was purified by silica chromatography (isohexane/ethyl acetate=4/1) yielding 0.62 g of 4-(tetrahydropyran-4-yloxy)-benzenesulfonyl chloride as a colorless oil. EI-MS: 276 (M+).

WORKUP

后处理

  1. temperatureto warm to −40° C.
  2. stirringStirring
  3. waitwas continued for 1 hour at −30° C. and subsequently for another hour at 5° C
  4. additionThe mixture was poured on ice
  5. extractionextracted with diethyl ether
  6. extractionthe ether extract
  7. washwashed with cold water and brine
  8. dry with materialdried (sodium sulfate)
  9. concentrationconcentrated
  10. customThe residue was purified by silica chromatography (isohexane/ethyl acetate=4/1)