HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Fluorophenyl)-2-methylpropan-1-one → 2-(4-Fluorophenyl)-2-methoxy-3,3-dimethyloxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Fluorophenyl)-2-methylpropan-1-one | HCID 2782829 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-Bromo-1-(4-fluorophenyl)-2-methylpropan-1-one | HCID 13113175 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4-Fluorophenyl)-2-methoxy-3,3-dimethyloxirane | HCID 13113176 | — |
Reaction Steps
39.22 g (0.16 mol) of 2-bromo-1-(4-fluorophenyl)-2-methylpropan-1-one, prepared by brominating 1-(4-fluorophenyl)-2-methylpropan-1-one analogously to European Patent Application No. 3,002, are dissolved in 50 ml of methanol. 23.5 g (0.176 mol) of methanolic 30% strength sodium methylate solution are added dropwise at room temperature. The methanol is then distilled off, and the residue is taken up with diethyl ether. The salt is filtered off, and the ether solution is concentrated. The liquid crude product is further reacted as described hereinafter without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04992547 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-77edb3ca03424b5092040fd7a2dc2e71 |
| Source note | uspto-grants-1991_02 |