HRID1464528

反应详情

EQUATION

反应方程式

HRID 1464528 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-12.5 °C

PROCEDURE

实验过程

A 2.1 ml (3.0×1.1 mmole) portion of n-butyllithium·hexane solution was added dropwise to a solution of 0.50 ml (3.0×1.2 mmole) of diisopropylamine in anhydrous tetrahydrofuran (5 ml) under an atmosphere of argon at -20° C. over the period of 5 minutes, followed by stirring at -20 to -5° C. for 10 minutes. The mixed solution was cooled at -20° C. and a solution of 0.38 g (3.0×1.1 mmole) of ethyl isobutyrate in tetrahydrofuran (4 ml) was added dropwise to it over the period of 5 minutes, followed by stirring at -20° to -5° C. for 20 minutes. A solution of 1.36 g (3.0 mmole) of 1-iodo-5-(2,5-dimethoxy-3,4,6-trimethylphenyl)-5-phenylpentane in tetrahydrofuran (14 ml) was added dropwise to the mixed solution over the period of 5 minutes, followed by stirring at -20° to -10° C. for 1.5 hours. After the reaction solution was cooled with ice, the reaction was suspended by adding 1N hydrochloric acid, and isopropyl ether and sodium chloride were added to extract the product. The organic layer was separated out, washed with aqueous saturated sodium chloride solution, dried (magnesium sulfate) and evaporated. The residual solution was chromatographed on a silica gel column to perform purification (elution with hexane/isopropyl ether) to thereby give 1.20 g (91%) of ethyl 7-(2,5-dimethoxy-3,4,6-trimethylphenyl)-2,2-dimethyl-7-phenylheptanoate. Its typical physical properties and nuclear magnetic resonance spectrum data are shown in Table 14.

WORKUP

后处理

  1. temperatureThe mixed solution was cooled at -20° C.
  2. stirringby stirring at -20° to -5° C. for 20 minutes
  3. stirringby stirring at -20° to -10° C. for 1.5 hours
  4. temperatureAfter the reaction solution was cooled with ice
  5. additionwere added
  6. extractionto extract the product
  7. customThe organic layer was separated out
  8. washwashed with aqueous saturated sodium chloride solution
  9. dry with materialdried (magnesium sulfate)
  10. customevaporated
  11. customThe residual solution was chromatographed on a silica gel column
  12. custompurification (elution with hexane/isopropyl ether)