Piperonal → Bis(3,4-methylenedioxy)chalcone

HRID 2074988

Reaction equation

HRID 2074988 reaction equation
[CH:1]1[C:6]([CH:7]=[O:8])=[CH:5][C:4]2[O:9][CH2:10][O:11][C:3]=2[CH:2]=1.[CH3:12][C:13]([C:15]1[CH:20]=[CH:19][C:18]2[O:21][CH2:22][O:23][C:17]=2[CH:16]=1)=O.[OH-].[Na+]>C(O)C>[CH2:22]1[O:21][C:18]2[CH:19]=[CH:20][C:15]([CH:13]=[CH:12][C:7]([C:6]3[CH:1]=[CH:2][C:3]4[O:11][CH2:10][O:9][C:4]=4[CH:5]=3)=[O:8])=[CH:16][C:17]=2[O:23]1

Participants

5

Reactant 3

HCID 8438PiperonalHCID 14798Sodium HydroxideHCID 76622Acetopiperone

Product 1

HCID 294346Bis(3,4-methylenedioxy)chalcone

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of piperonal (460 mg) and 3,4-methylenedioxyacetophenone (500 mg) in ethanol (20 ml) was treated with 1M NaOH solution (4 ml), then the mixture was stirred overnight. The pale yellow crystalline solid was filtered off, washed with water then cold aqueous ethanol and dried to give pure bis(3,4-methylenedioxy)chalcone DC-0006B (476 mg, 53%).

Workup

  1. filtrationThe pale yellow crystalline solid was filtered off
  2. washwashed with water
  3. dry with materialcold aqueous ethanol and dried

Sources & evidence

ORD record
ord-f8e0be31c7fd457bab9fcd8882d14a3f
Source dataset
uspto-grants-2011_04
Patent number
US07919530B2

Linked notes

Loading…