HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-[5-Fluoro-2-(2,2,2-trifluoroethoxy)phenyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bis(2-chloroethyl)amine hydrochloride | HCID 522769 | — |
| Reactant | 5-Fluoro-2-(2,2,2-trifluoroethoxy)aniline | HCID 17485413 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 1-[5-Fluoro-2-(2,2,2-trifluoroethoxy)phenyl]piperazine | HCID 23447904 | 14.5% |
Reaction Steps
A stirred mixture of 0.52 g of Compound 8B, 0.45 g of 98% bis-(2-chloroethyl)amine hydrochloride, 0.5 g of potassium iodide, 0.34 g of anhydrous potassium carbonate and 20 mL of n-butanol was refluxed for 32 hours under nitrogen. The solvent was removed under reduced pressure; the residue was treated with 10 mL of water and 10 mL of 20% aqueous sodium carbonate and extracted with 2×30 mL of ethyl acetate. The organic layer was washed with brine, dried over sodium sulphate and evaporated to dryness in vacuo. The residue was purified by flash chromatography (chloroform/2N ammonia solution in methanol, gradient from 100:3to 100:5) to afford 0.1 g (14%) of Compound 8C as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403594B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-5efd4545792a47d1ad9937e5a9160a47 |
| Source note | uspto-grants-2002_06 |