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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | 1-(2-chloroethyl)-1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran | HCID 20087957 | — |
| Reactant | 1-(4,4-Diphenylbutyl)piperazine hydrochloride | HCID 20087966 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[2-(1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran-1-yl)ethyl]-4-(4,4-diphenylbutyl)piperazine (E)-2-butenedioate | HCID 86747155 | 35.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05393759 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-249b47e655fc461abf0176b2f56b5d6e |
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| Source note | uspto-grants-1995_02 |
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