HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-(3-Methoxy-2-methylphenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Methoxy-2-MethylBenzoic Acid | HCID 7021483 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Catalyst | Iron (III) acetylacetonate | HCID 11110968 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 1-(3-Methoxy-2-methylphenyl)ethanone | HCID 19702342 | — |
Reaction Steps
A solution of 2-methyl-3-methoxybenzoic acid (10.0 g, 60.2 mmol) in thionyl chloride (50 ml) was heated at reflux for 1 h and then cooled and concentrated in vacuo. To the residue was added tetrahydrofuran (100 ml) and iron (III) acetylacetonate (638 mg, 1.8 mmol) and the solution was cooled to −20° C., before addition of methylmagnesium bromide (3M in diethyl ether, 22.1 ml, 66.2 mmol). After stirring for 15 min, the mixture was poured into saturated aqueous ammonium chloride solution and extracted with dichloromethane. The combined extracts were washed with saturated aqueous sodium hydrogen carbonate solution, dried (MgSO4) and concentrated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592362B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-99abc8a9768d498693285ed446c76140 |
| Source note | uspto-grants-2009_09 |