HRID29133

反应详情

EQUATION

反应方程式

HRID 29133 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

As shown in Scheme IV, in this method, adamantyl bromide (Formula A) is alkylated via zinc chloride catalysis to produce <a-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid (Formula B). <a-Hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid (Formula B) is then esterified using acetyl chloride in methanol to produce <a-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid, methyl ester (Formula C). <a-Hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid, methyl ester (Formula C) is then converted to <a-oxotricyclo[3.3.1.13,7]decane-1-acetic acid, methyl ester (Formula D) by Swern oxidation. <a-Oxotricyclo[3.3.1.13,7]decane-1-acetic acid, methyl ester (Formula D) is then hydroxylated to form 3-hydroxy-<a-oxotricyclo[3.3.1.13,7]decane-1-acetic acid, methyl ester (Formula I), which is then hydrolyzed to form 3-hydroxy-<a-oxotricyclo[3.3.1.13,7]decane-1-acetic acid (Formula II). Also see Examples 21 through 25 herein.