HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 4-methyl-5-(oxiran-2-yl)isobenzofuran-1(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4-methyl-5-vinylisobenzofuran-1(3H)-one | HCID 66643922 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-methyl-5-(oxiran-2-yl)isobenzofuran-1(3H)-one | HCID 55270555 | — |
Reaction Steps
5-ethenyl-4-methyl-2-benzofuran-1(3H)-one (1.5 g, 8.4 mmol) was added to DCM (25 mL) at 0° C. then meta-chloroperbenzoic acid (2.9 g, 17 mmol) was added and the mixture was stirred at room temperature overnight. The reaction mixture was washed once each with saturated aqueous Na2S2O3, saturated sodium bicarbonate, and brine. The organic layer was dried over Na2SO4, filtered, and evaporated to dryness. The crude material was purified by MPLC chromatography (eluting with 0-80% EtOAc/hexane solvent system) to yield 4-methyl-5-oxiran-2-yl-2-benzofuran-1(3H)-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108947B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-6d2fc5545159459da5eddd34c1e521c4 |
| Source note | uspto-grants-2015_08 |