反应 #943990

ord-bd9f9db7a27c45a0b9426657f17c0f43

反应方程式

Br
HBr
COc1c(O)ccc2c1CCC(c1ccccc1)C2c1ccc(OCCN2CCCC2)cc1
1-methoxy-6-phenyl-5-[4-(2-pyrroldin-1-yl-ethoxy)-phenyl]-5,6,7,8-tetrahydro-naphthalen-2-ol
CC(=O)O
HOAc
COc1ccc2c(c1OC)CCC(c1ccccc1)C2c1ccc(OCCN2CCCC2)cc1
1-{2-[4-(5,6-dimethoxy-2-phenyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-ethyl}-pyrrolidine

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Using a procedure analogous to Example 5, from 2.3 g (0.005 mole) of 1-{2-[4-(5,6-dimethoxy-2-phenyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-phenoxy]-ethyl}-pyrrolidine, 80 ml of HOAc and 80 ml of 48% aqueous HBr, was obtained 650 mg of a mixture of 2-methoxy-6-phenyl-5-[4-(2-pyrrolidin-1-yl-ehtoxy)-phenyl]-5,6,7,8-tetrahydro-naphthalen-1-ol and 1-methoxy-6-phenyl-5-[4-(2-pyrroldin-1-yl-ethoxy)-phenyl]-5,6,7,8-tetrahydro-naphthalen-2-ol.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE039419E1uspto-grants-2006_12