HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 2-(3-Methylphenyl)acetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | m-Xylyl bromide | HCID 12099 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3-Methylphenyl)acetophenone | HCID 13173614 | — |
Reaction Steps
A solution of benzonitrile (58.5 g) in anhydrous ether (150 ml) is added dropwise with stirring to Grignard reagent which is prepared from magnesium turnings (14.6 g), a small amount of iodine and m-methylbenzylbromide (100 g) in anhydrous ether (800 ml) at moisture-free atmosphere. The mixture is refluxed for 6 hours. The reaction mixture is decomposed by adding water thereto, and the ether layer is separated and distilled to remove the solvent. The residue is mixed with 10% hydrochloric acid and the mixture is refluxed for 1.5 hours. After cooling, the mixture is extracted with ether. The ether layer is dried over anhydrous sodium sulfate and the solvent is distilled off to give crude m-methylbenzyl phenyl ketone (82 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04080453 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-f088f7247eec463997aef09cbab947cb |
| Source note | uspto-grants-1978_03 |