反应 #470420

ord-aefc2a68443641af869a4e1bf1d52239

反应方程式

Oc1ccc(C2=Cc3ccc(O)cc3OC2)cc1
4′,7-Dihydroxyisoflav-3-ene
Cc1ccc(N)cc1
p-toluidine
CCO
ethanol
C=O
Formaldehyde
Cc1ccc(N2COc3cc4c(cc3C2)C=C(c2ccc(O)cc2)CO4)cc1
title compound
收率 22.0%
Cc1ccc(N2COc3cc4c(cc3C2)C=C(c2ccc(O)cc2)CO4)cc1
4-(3-p-Tolyl-2,3,4,8-tetrahydrochromeno[6,7-e][1,3]oxazin-7-yl)phenol
收率 22.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The resulting precipitate was collected

实验过程

4′,7-Dihydroxyisoflav-3-ene (499 mg, 2.08 mmol) and p-toluidine (290 mg, 2.71 mmol) were dissolved in ethanol (8 ml). Formaldehyde solution (2 ml, 0.03 mol, 37% wt) was added and the reaction stirred at room temperature for 2 days. The resulting precipitate was collected to afford the title compound (167 mg, 22%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08367659B2uspto-grants-2013_02