HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bisphenol A diglycidyl ether diacrylate → 2-(4-Fluorophenyl)-2-methoxy-3,3-dimethyloxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bisphenol A diglycidyl ether diacrylate | HCID 92212 | — |
| 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 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 2-(4-Fluorophenyl)-2-methoxy-3,3-dimethyloxirane | HCID 13113176 | — |
Reaction Steps
100.32 g (0.41 mol) of 2-bromo-1-(4-fluorophenyl)-2-methylpropan-1-one, prepared by brominating 1-(4-fluorophenyl)-2-methylpropan-1-one (as is described in EP-A-3002), are dissolved in 80 ml of dry methanol and 24.3 g (0.45 mol) of sodium methoxide in a solvent mixture of 60 ml dry methanol and 120 ml of chlorobenzene are added dropwise at 20° C. The methanol is then distilled off and the chlorobenzene solution is concentrated. The liquid crude product (90.8 g) is further purified by distillation at 60° C. and 0.2 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06022906 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-53e21ef81ad649b19a9efa67caf37ef5 |
| Source note | uspto-grants-2000_02 |