反応 #470411

ord-b6c6448adf474d74b28f8268ff7e64f2

反応方程式

Oc1ccc(C2=Cc3ccc(O)cc3OC2)cc1
4′,7-Dihydroxyisoflav-3-ene
CCO
ethanol
CNCc1ccccc1
methylbenzylamine
C=O
formaldehyde
Oc1ccc(C2=Cc3ccc(O)cc3OC2)cc1
dehydroequol
CCO
ethanol
CC(c1ccccc1)N1COc2cc3c(cc2C1)C=C(c1ccc(O)cc1)CO3
title compound
CC(c1ccccc1)N1COc2cc3c(cc2C1)C=C(c1ccc(O)cc1)CO3
4-(3-(1-Phenylethyl)-2,3,4,8-tetrahydrochromeno[6,7-e][1,3]oxazin-7-yl)phenol

反応条件

温度
85°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction mixture was refluxed for approximately 7 hours
  2. 2
    温度after cooling to room temperature the volume
  3. 3
    濃縮was concentrated in vacuo
  4. 4
    workup.WAITThe mixture was left in the fridge
  5. 5
    その他to crystallise
  6. 6
    その他The yellow solid was collected under suction
  7. 7
    その他the filtrate evaporated to dryness

実験手順

4′,7-Dihydroxyisoflav-3-ene (0.45 g, 1.87 mmol) was dissolved in ethanol (ca 40 mL) and heated to 80-90° C. A solution of methylbenzylamine (0.44 mL, 4.03 mmol) and 37% formaldehyde (0.35 mL, 123 mmol) in ethanol (ca. 20 mL) was added to the dehydroequol solution. The reaction mixture was refluxed for approximately 7 hours and after cooling to room temperature the volume was concentrated in vacuo. The mixture was left in the fridge to crystallise. The yellow solid was collected under suction and the filtrate evaporated to dryness to obtain a second crop of the title compound, (combined yield 0.17 g, 23%).

出典

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