HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 21883828, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 4'-Hydroxyacetophenone | HCID 7469 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Bis(bromomethyl)benzene | HCID 69335 | — |
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 21883828 | HCID 21883828 | — |
Reaction Steps
α,α′-Dibromo-para-xylene (30 mmol), 4-hydroxyacetophenone (20 mmol), and potassium carbonate (50 mmol) were refluxed in 50 ml of acetone for 12 hours. The solvent was removed under reduced pressure and the residue purified by column chromatography on silica gel (eluent: methylene chloride/petroleum ether/methanol (60/38/2)). The product (2 mmol), 4-methylpiperidine (6 mmol), potassium carbonate (8 mmol), and catalytic amounts of potassium iodide were refluxed in acetone for 12 hours. The solvent was evaporated. The residue was washed with water and extracted with ethyl acetate. The solvent was removed under reduced pressure. The product was crystallized with oxalic acid from diethyl ether/ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138413B1 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-f157ccc62ded4188a1b987ab0f56ebbb |
| Source note | uspto-grants-2006_11 |