HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Hydrochloric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(p-Tolyl)piperazine | HCID 83113 | — |
| Reactant | HCID 14422830 | HCID 14422830 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 19840251 | HCID 19840251 | — |
Reaction Steps
This compound was prepared according to the procedure of Example 25. A mixture of 1.8 g (0.01 mole) of 1-(4-methylphenyl)piperazine, 2.2 g (0.01 mole) of 4-chloro-1-(4-fluorophenoxy)-2-butanol, 5.2 g (0.05 mole) of anhydrous sodium carbonate, and 0.1 g of potassium iodide in a total volume of 200 ml of 1-butanol gave a golden oil as residue. The hydrochloride was formed in 2-propanol saturated with hydrogen chloride and the collected solid was recrystallized from methanol-water-ethyl ether to give 1.8 g (41%) of white solid, m.p. 200°-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04882330 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-cacceb7ea78b46b2ac7d14254d866bb8 |
| Source note | uspto-grants-1989_11 |