Reaction #470411

ord-b6c6448adf474d74b28f8268ff7e64f2

Reaction equation

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

Conditions

Temperature
85°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureThe reaction mixture was refluxed for approximately 7 hours
  2. 2
    Temperatureafter cooling to room temperature the volume
  3. 3
    Concentrationwas concentrated in vacuo
  4. 4
    workup.WAITThe mixture was left in the fridge
  5. 5
    Otherto crystallise
  6. 6
    OtherThe yellow solid was collected under suction
  7. 7
    Otherthe filtrate evaporated to dryness

Procedure

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%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08367659B2uspto-grants-2013_02