HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-[2-(1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran-1-yl)ethyl]-4-[3,3-bis (4-fluorophenyl)propyl]piperazine (E)-2-butenedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-[3,3-Bis(4-fluorophenyl)propyl]piperazine | HCID 13883282 | — |
| Reactant | 1-(2-chloroethyl)-1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran | HCID 20087957 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[2-(1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran-1-yl)ethyl]-4-[3,3-bis (4-fluorophenyl)propyl]piperazine (E)-2-butenedioate | HCID 67784700 | 61% |
Reaction Steps
A mixture of 8,6 of 1-(2-chloroethyl)-1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran, 8 g of 1-[3,3-bis(4-fluorophenyl)propyl]piperazine, 5,2 g of potassium carbonate and 0,4 g of potassium iodide in 100 ml of dimethylformamide was refluxed for 4 h. Water was added and the base was extracted twice with ethyl acetate. After washing, drying and evaporation the difumarate was prepared in absolute ethanol to yield 13,2 g (61,2%) of 1-[2-(1-ethyl-3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran-1-yl)ethyl]-4-[3,3-bis-(4-fluorophenyl)propyl]piperazine (E)-2-butenedioate (1:2) salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05238939 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-ebcf99f086e64beeb02b277b34addfc9 |
| Source note | uspto-grants-1993_08 |