HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848426Generated: October 31, 2026
m-Chloroperbenzoic acid → HCID 77231249, compound
https://huagongshe.com/reaction/1848426
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 66646404 | HCID 66646404 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 77231249 | HCID 77231249 | — |
Reaction Steps
5-Ethenyl-4-(2-hydroxyethyl)-2-benzofuran-1(3H)-one (1.2 g, 5.9 mmol) was added to a flask containing a stir bar. To the flask was then added dichloromethane (20 mL). The flask was placed in a cool bath of 0° C.; to the flask was poured mCPBA (1.5 g, 8.8 mmol) and the resulting mixture was stirred at room temperature for overnight; LC as well as TLC (hexanes/EtOAc=1/1) indicated that reaction had gone to completion. The solution was treated with dichloromethane and washed with NaHCO3, Na2S2O3, and water, the organic layer was then dried over Na2SO4, filtered and concentrated to dryness, it was then treated with AcOH (20 mL) and stirred overnight; LC indicated formation of cyclized product. The solvent was removed and the resulting residue was absorbed onto silica gel and the title compound was isolated with the solvent system of hexanes/EtOAc (1/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08952166B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-85902392cce74aef81a618579c5ec7c3 |
|---|
| Source note | uspto-grants-2015_02 |
|---|