HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → 2-[(4-Benzoylphenoxy)methyl]oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxybenzophenone | HCID 14347 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-[(4-Benzoylphenoxy)methyl]oxirane | HCID 352816 | — |
Reaction Steps
As illustrated in FIG. 6, 100 mL of dried acetone were added to a dry, 250-mL round bottom flask, equipped with a magnetic stirrer, along with 15.05 grams of 4-hydroxybenzophenone, 32.1 grams of epichlorohydrin, and 6.2 grams of potassium carbonate. The solution was heated to reflux for 6 hours and then cooled to room temperature. The precipitated potassium chloride was filtered off, and the solution was evaporated to remove excess epichlorohydrin. The crude product was recrystallized from methanol. 1H NMR data confirmed the formation of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07045366B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-11abb5634ed142ee9bd12b16b8fc0da6 |
| Source note | uspto-grants-2006_05 |