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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170272Generated: October 30, 2026

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

https://huagongshe.com/reaction/2170272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactant1,3-Benzodioxole, 5-(chloromethyl)-HCID 88713—
SolventDimethylformamideHCID 6228—
ProductPiperazine, 1,4-bis(1,3-benzodioxol-5-ylmethyl)-HCID 96702—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051253B2
Source datasetuspto-grants-2015_06
ORD IDord-7f8d9b1c9d8a43a0bf2872185d02dcc0
Source noteuspto-grants-2015_06