HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Ethanone, 2-iodo-1-(4-methoxyphenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethanone, 2-iodo-1-(4-methoxyphenyl)- | HCID 144919 | 94% |
Reaction Steps
A mixture of 2-bromo-1-(4'-methoxy-phenyl)-ethanone (22.9 g, 0.1 mol), potassium iodide (66.4 g, 0.4 mol) and acetone (200 ml) is heated at reflux for 3 h. The reaction mixture is cooled, poured into water (0.25 l) and extracted with ethyl ether (3×100 ml) The combined organic extract is washed with water and dried (Na2SO4). Evaporation of the solvent in vacuo leaves a residue which by crystallization from petroleum ether gives 2-iodo-1-(4'-methoxy-phenyl)-ethanone (22 g, 0.094 mol, yield 80%), m.p. 63°-65° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04748253 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-fb7353a0857e4bc3af4dd9d29c2c5cfe |
| Source note | uspto-grants-1988_05 |