HRID1639440
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
PROCEDURE
实验过程
Using the procedure of Step F of Example 9, (IR, cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2-fluoroethoxy)-1-propenyl]-cyclopropane-carboxylic acid and α-ethynyl-3-phenoxy-benzyl alcohol were reacted to obtain α-ethynyl-3-phenoxy-benzyl (IR,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2-fluoroethoxy) -1-propenyl]-cyclopropane-carboxylate with a specific rotation of [α]D20= +47° ±1.5° (c=1% in CHCl3).
WORKUP
后处理
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