Piperazine → Piperazine, 1,4-bis(1,3-benzodioxol-5-ylmethyl)-

HRID 1819979Notes

Reaction equation

HRID 1819979 reaction equation
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[H-].[Na+].[CH2:9]1[O:19][C:18]2[CH:17]=[CH:16][C:13]([CH2:14]Cl)=[CH:12][C:11]=2[O:10]1.[OH-:20].[Na+]>CN(C=O)C>[CH2:9]1[O:19][C:18]2[CH:17]=[CH:16][C:13]([CH2:14][N:1]3[CH2:6][CH2:5][N:4]([CH2:14][C:13]4[CH:16]=[CH:17][C:18]5[O:20][CH2:9][O:10][C:11]=5[CH:12]=4)[CH2:3][CH2:2]3)=[CH:12][C:11]=2[O:10]1

Participants

6

Reactant 4

HCID 4837PiperazineHCID 14798Sodium HydroxideHCID 24758Sodium hydrideHCID 887131,3-Benzodioxole, 5-(chloromethyl)-

Product 1

HCID 96702Piperazine, 1,4-bis(1,3-benzodioxol-5-ylmethyl)-

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

To a solution of piperazine (207 mg) in dry DMF (5 ml) under nitrogen was added sodium hydride (80% w/w in oil 250 mg), followed by 3,4-methylenedioxybenzylchloride (0.90 g) and the mixture stirred at room temperature overnight. Aqueous NaOH (50 ml, 1M) was added slowly, then saturated NaCl solution (50 ml) and the product extracted with dichloromethane (2×100 ml). The organic layer was washed with water (2×100 ml), dried and evaporated in vacuo to give a white solid. Column chromatography eluting with increasing proportions of ether in dichloromethane gave pure DC-0009B (0.68 g, 80%) as a white powder.

Workup

  1. extractionsaturated NaCl solution (50 ml) and the product extracted with dichloromethane (2×100 ml)
  2. washThe organic layer was washed with water (2×100 ml)
  3. customdried
  4. customevaporated in vacuo
  5. customto give a white solid
  6. washColumn chromatography eluting with increasing proportions of ether in dichloromethane
  7. customgave pure DC-0009B (0.68 g, 80%) as a white powder

Sources & evidence

ORD record
ord-57fb8cbf7a50420da2cc2f2361a778eb
Source dataset
uspto-grants-2009_10
Patent number
US07601876B2

Reaction notes

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