反应 #1238

ord-f03bd0e627354ee4a55f5536f5f04cf4

反应方程式

Oc1cc2ccc(Br)cc2cc1C12CC3CC(CC(C3)C1)C2
7-(1-adamantyl)-6-hydroxy-2-bromonaphthalene
Fc1ccc(CBr)cc1
4-fluorobenzyl bromide
Fc1ccc(COc2cc3ccc(Br)cc3cc2C23CC4CC(CC(C4)C2)C3)cc1
expected compound
收率 86.0%
Fc1ccc(COc2cc3ccc(Br)cc3cc2C23CC4CC(CC(C4)C2)C3)cc1
7-(1-adamantyl)-6-(4-fluorobenzyl)oxy-2-bromonaphthalene
收率 86.0%

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Following the basic procedure of Example 11, by reacting 1.1 g (3 mmol) of 7-(1-adamantyl)-6-hydroxy-2-bromonaphthalene with 420 μl (3,3 mmol) of 4-fluorobenzyl bromide, 1.2 g (86%) of the expected compound was obtained in the form of a colorless oil.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723499uspto-grants-1998_03