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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369767Generated: 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/369767

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 numberUS06140331
Source datasetuspto-grants-2000_10
ORD IDord-a9408372408f465faf1f6e2346ffb2fa
Source noteuspto-grants-2000_10