反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- additionwith internal temperature probe/nitrogen inlet and addition funnel
- additionadd at a rate such that the internal temperature
- customdoes not reach above −60° C
- additionAfter the addition
- customthe reaction
- stirringto stir at −25° C. for 30 min
- temperaturethen cool to about −60° C
- additionAfter the addition
- customto a −10° C.
- temperaturemaintain the internal reaction temperature below 10° C. for 1 hr
- temperatureCool the mixture to 0° C.
- customthen quench with 2 L aqueous 1N hydrochloric acid
- additionTransfer the mixture to a 22 L separatory funnel and dilute with 2.5 L water and 2 L ether
- customSeparate the layers
- extractionextract the aqueous layer with ether
- dry with materialDry the combined organic phase over anhydrous magnesium sulfate
- filtrationfilter
- concentrationconcentrate to 800 g of a thick oil
- customPurify by silica gel chromatography