HRID37035

反应详情

EQUATION

反应方程式

HRID 37035 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
10 °C

PROCEDURE

实验过程

A solution of lithium bis(trimethylsilyl)amide was prepared by adding 2.5M n-butyl lithium (208 mL) to a solution of 1,1,1,3,3,3-hexamethyldisilazane (110 mL, 0.52 mol) in tetrahydrofuran (THF) (140 mL) at 0° C. After stirring for 15 min, this solution was added via a cannula to a solution of p-tolualdehyde (59 mL, 0.5 mol) in THF (100 mL), while keeping the temperature between -40° and -50° C. The reaction mixture was then allowed to warm to 10° C. over 30 min. A 2M solution of allyl magnesium chloride (260 mL) in THF was added, keeping the temperature between 10° and 15° C. After stirring for 30 min the reaction was poured into a solution of ammonium chloride (150 gm) in water (1 L). The layers were separated and the aqueous layer was extracted with ether/hexane. The organic layers were washed with brine, combined, dried over sodium sulfate and evaporated. The residue was added to a solution of (1R)-(-)-10-camphorsulfonic acid (62.5 gm) in ethyl acetate (1 L) with cooling. On standing overnight at rt, crystals formed which were filtered and washed with ethyl acetate. The crystals were then stirred with refluxing ethyl acetate (300 mL), filtered and washed with ethyl acetate. The pure title compound weighed 60.7 gm. [α]D =-27.16 (c=0.5, 100% EtOH).

WORKUP

后处理

  1. customthe temperature between -40° and -50° C
  2. customthe temperature between 10° and 15° C
  3. stirringAfter stirring for 30 min the reaction
  4. customThe layers were separated
  5. extractionthe aqueous layer was extracted with ether/hexane
  6. washThe organic layers were washed with brine
  7. dry with materialdried over sodium sulfate
  8. customevaporated
  9. additionThe residue was added to a solution of (1R)-(-)-10-camphorsulfonic acid (62.5 gm) in ethyl acetate (1 L)
  10. temperaturewith cooling
  11. waitOn standing overnight at rt
  12. customcrystals formed which
  13. filtrationwere filtered
  14. washwashed with ethyl acetate
  15. stirringThe crystals were then stirred with refluxing ethyl acetate (300 mL)
  16. filtrationfiltered
  17. washwashed with ethyl acetate