反应 #1493508

ord-26f5b27584654db69f93d572ef67063c

反应方程式

Oc1ccccc1O
catechol
OC1C2CC3CC(C2)CC1(O)C3
adamantane diol
O
Water
Oc1ccc(C23CC4CC(C2)CC(c2ccc(O)c(O)c2)(C4)C3)cc1O
product
Oc1ccc(C23CC4CC(C2)CC(c2ccc(O)c(O)c2)(C4)C3)cc1O
1,3 bis (3,4 dihydroxyphenyl) adamantane

反应条件

温度
80°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取the mixture extracted into 10% methanol in chloroform which
  2. 2
    其他was dried
  3. 3
    其他evaporated in vacuo
  4. 4
    其他to give a white solid
  5. 5
    其他Purification by column chromatography over silica gel eluting with 0-20% methanol in chloroform

实验过程

According to the method described by Lu a solution of catechol (1.0 g) and adamantane diol (0.5 g) in methanesulfonic acid (2 ml) was heated to 80° C. for 3 hours, then left at room temperature overnight. Water was added and the mixture extracted into 10% methanol in chloroform which was dried and evaporated in vacuo to give a white solid. Purification by column chromatography over silica gel eluting with 0-20% methanol in chloroform gave the product as a white solid. Crystallisation from diethyl ether/40% petroleum ether then gave the pure product 10 as a white crystalline solid (210 mg, 20%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08916598B2uspto-grants-2014_12