HRID1160251

反应详情

EQUATION

反应方程式

HRID 1160251 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-75 °C

PROCEDURE

实验过程

Stir a mixture of (R)-4-benzyl-3-pent-4-enoyl-oxazolidin-2-one (345 g, 1.33 mol) and THF (1.8 L) in a 12 L 3-neck round bottom flask, with internal temperature probe/nitrogen inlet and addition funnel, under a nitrogen atmosphere and cool to −75° C. Transfer 1 M LiHMDS (1.6 L) to the addition funnel and add at a rate such that the internal temperature does not reach above −60° C. After the addition is complete, allow the reaction to stir at −25° C. for 30 min then cool to about −60° C. At this point add solid 2-bromomethyl-1,3-dichloro-5-benzyloxy-benzene portionwise over 5 min. After the addition is complete, transfer the reaction vessel to a −10° C. acetone bath and maintain the internal reaction temperature below 10° C. for 1 hr. Cool the mixture to 0° C. then quench with 2 L aqueous 1N hydrochloric acid. Transfer the mixture to a 22 L separatory funnel and dilute with 2.5 L water and 2 L ether. Separate the layers and extract the aqueous layer with ether. Dry the combined organic phase over anhydrous magnesium sulfate, filter and concentrate to 800 g of a thick oil. Purify by silica gel chromatography using hexanes:ethyl acetate to obtain 597 g, (86%) of a colorless oil.

WORKUP

后处理

  1. additionwith internal temperature probe/nitrogen inlet and addition funnel
  2. additionadd at a rate such that the internal temperature
  3. customdoes not reach above −60° C
  4. additionAfter the addition
  5. customthe reaction
  6. stirringto stir at −25° C. for 30 min
  7. temperaturethen cool to about −60° C
  8. additionAfter the addition
  9. customto a −10° C.
  10. temperaturemaintain the internal reaction temperature below 10° C. for 1 hr
  11. temperatureCool the mixture to 0° C.
  12. customthen quench with 2 L aqueous 1N hydrochloric acid
  13. additionTransfer the mixture to a 22 L separatory funnel and dilute with 2.5 L water and 2 L ether
  14. customSeparate the layers
  15. extractionextract the aqueous layer with ether
  16. dry with materialDry the combined organic phase over anhydrous magnesium sulfate
  17. filtrationfilter
  18. concentrationconcentrate to 800 g of a thick oil
  19. customPurify by silica gel chromatography