HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 1-[2-(4-Bromophenyl)-2-oxoethyl]pyridin-1-ium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[2-(4-Bromophenyl)-2-oxoethyl]pyridin-1-ium iodide | HCID 13552281 | 76% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To 10.0 g of 4′-bromoacetophenone were added 12.8 g of iodine and 80 mL of pyridine and heated, and the mixture was stirred at 100° C. for 3 hours. After cooling to room temperature, 100 mL of water was added, and purification was performed by recrystallization. Drying was performed under reduced pressure at 70° C. for 12 hours to give 15.5 g (yield: 76%) of 4-bromophenacylpyridinium iodide as a brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08771841B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-6eeaeeb0d1ad442498ff417d3a600cf2 |
| Source note | uspto-grants-2014_07 |