HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 86747157, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(4,4-Bis(4-fluorophenyl)butyl)piperazine | HCID 79729 | — |
| Reactant | HCID 20087933 | HCID 20087933 | — |
| Product | HCID 86747157 | HCID 86747157 | — |
Reaction Steps
A mixture of 7,6 g of known 1-(2-chloroethyl)-1-ethyl-3,4-dihydro-6-methoxy-1H-2-benzopyran, 9 g of 1-[4,4-bis(4-fluorophenyl)butyl]piperazine, 0,4 g of potassium iodide, and 5 g of potassium carbonate in 100 ml of dimethylformamide was refluxed for 6 h. After hydrolysis the mixture was extracted with dimethyl ether, and the ethereal phase was washed, dried, and evaporated. The base was precipitated and the dimaleate salt was prepared in ethanol and recrystallized from ethanol-water (3:1) to give 13,8 g of 1-[2-(1-ethyl-3,4-dihydro-6-methoxy-1H-2-benzopyran-1-yl)ethyl]-4-[4,4-bis(4-fluorophenyl)butyl]piperazine (Z)-2-butenedioate (1:2) salt. mp 184° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05238939 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-f1e66de32e494ad1b42cf31855e8d646 |
| Source note | uspto-grants-1993_08 |