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-(4-Chlorophenyl)piperazine | HCID 97478 | — |
| Reactant | 4-Chloro-1-(4-chlorophenoxy)-2-butanol | HCID 13120349 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 14422865 | HCID 14422865 | — |
Reaction Steps
This compound was prepared according to the procedure of Example 97. A mixture of 3.2 g (0.016 mole) of 1-(4-chlorophenyl)piperazine, 3.8 g (0.016 mole) of 4-chloro-1-(4-chlorophenoxy)-2-butanol, 8.3 g (0.078 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 methol-water-ethyl ether to give 3.6 g (47%) of white solid, m.p. 195°-200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04806555 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-fda09097e9af4840ac19806f89bd757c |
| Source note | uspto-grants-1989_02 |