HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 2-Benzoyl-8-[2-chloro-4-methoxyphenoxy]-1-phenyl-1-octanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dibenzoylmethane | HCID 8433 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-((6-Bromohexyl)oxy)-3-chloroanisole | HCID 92068 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 2-Benzoyl-8-[2-chloro-4-methoxyphenoxy]-1-phenyl-1-octanone | HCID 12733727 | 38.8% |
Reaction Steps
A mixture of 11.2 g (0.05 m) of dibenzoylmethane, 16.1 g (0.05 m) of 6-(2-chloro-4-methoxyphenoxy)hexyl bromide, 20.6 g (0.15 m) of milled potassium carbonate, 2.0 g of potassium iodide and 250 ml of 2-butanone was heated at reflux for 18 hours. The reaction mixture was filtered hot and concentrated to a brown oil. The latter was stirred with cold ether and seeded with a sample of the desired product having the m.p. 69°-70° C. The solid product thus obtained was collected to afford 9.0 g of 2-benzoyl-8-[2-chloro-4-methoxyphenoxy]-1-phenyl-1-octanone; MIC=3 microg/ml (herpes 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04209526 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-5fea07ff96914371b470ea13be954454 |
| Source note | uspto-grants-1980_06 |