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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275384Generated: October 31, 2026

Potassium Iodide → 1-[2-(1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran-1-yl)ethyl]-4-(4,4-diphenylbutyl)piperazine (E)-2-butenedioate

https://huagongshe.com/reaction/275384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantFumaric AcidHCID 444972—
Reactant1-(2-chloroethyl)-1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyranHCID 20087957—
Reactant1-(4,4-Diphenylbutyl)piperazine hydrochlorideHCID 20087966—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Product1-[2-(1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran-1-yl)ethyl]-4-(4,4-diphenylbutyl)piperazine (E)-2-butenedioateHCID 8674715535.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 8 g of 1-(4,4-diphenylbutyl)piperazine hydrochloride, 8.4 g of known 1-(2-chloroethyl)-1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran, 5,6 g of potassium carbonate and 1 g of potassium iodide in 100 ml of dimethylformamide was heated at 100° C. for 3 h. After hydrolysis the mixture was extracted twice with ethyl acetate, dried and concentrated. The difumarate salt was prepared by adding 14.6 g of fumaric acid to a solution of the free base in ethanol, to give 4.2 g (35.6%) of 1-[2-(1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran-1-yl)ethyl]-4-(4,4-diphenylbutyl)piperazine (E)-2-butenedioate (1:2) salt. mp 207.8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05393759
Source datasetuspto-grants-1995_02
ORD IDord-249b47e655fc461abf0176b2f56b5d6e
Source noteuspto-grants-1995_02