Reaction #470411
ord-b6c6448adf474d74b28f8268ff7e64f2
Reaction equation
4′,7-Dihydroxyisoflav-3-ene
ethanol
methylbenzylamine
formaldehyde
dehydroequol
ethanol
→
title compound
4-(3-(1-Phenylethyl)-2,3,4,8-tetrahydrochromeno[6,7-e][1,3]oxazin-7-yl)phenol
Reagents
None
Conditions
Temperature
85°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1TemperatureThe reaction mixture was refluxed for approximately 7 hours
- 2Temperatureafter cooling to room temperature the volume
- 3Concentrationwas concentrated in vacuo
- 4workup.WAITThe mixture was left in the fridge
- 5Otherto crystallise
- 6OtherThe yellow solid was collected under suction
- 7Otherthe 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%).