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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290782Generated: October 26, 2026

Potassium Iodide → 1-(1,4-Benzodioxan-5-yl)-4-(2-(2,2-dimethoxy-1-ethylamino)-1-ethyl)piperazine

https://huagongshe.com/reaction/1290782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
ReactantAcetaldehyde, bromo-HCID 105131—
Reactant1-(2-Amino-1-ethyl)-4-(1,4-benzodioxan-5-yl)piperazineHCID 10587641—
SolventWaterHCID 962—
SolventEthylacetate methanolHCID 21584119—
Product1-(1,4-Benzodioxan-5-yl)-4-(2-(2,2-dimethoxy-1-ethylamino)-1-ethyl)piperazineHCID 70290042—

Reaction Steps

A mixture of 1-(2-amino-1-ethyl)-4-(1,4-benzodioxan-5-yl)piperazine (9.1 g), bromoacetaldehyde dimethylacetale (6.5 g), potassium iodide (0.5 g), and potassium carbonate (4.8 g) in 1,4-dioxan (200 ml) was refluxed for 16 h. Water was added followed by extraction with ethyl acetate. The organic phase was concentrated in vacuo leaving an oil which was applied to a silica gel column (eluent: ethyl acetate/methanol=1:3). The product, 1-(1,4-benzodioxan-5-yl)-4-[2-(2,2-dimethoxy-1-ethylamino)-1-ethyl]piperazine, was obtained as an oil (4.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753661
Source datasetuspto-grants-1998_05
ORD IDord-0e54196d5bb04784812c649f9f2866f4
Source noteuspto-grants-1998_05