HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274213Generated: October 25, 2026
Ethanol → 1H-Indene-1,3(2H)-dione, 2-(3-methoxyphenyl)-
https://huagongshe.com/reaction/274213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Methoxybenzaldehyde | HCID 11569 | — |
| Reactant | 2(3H)-Benzofuranone | HCID 68382 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1H-Indene-1,3(2H)-dione, 2-(3-methoxyphenyl)- | HCID 2817810 | — |
Reaction Steps
Sodium (18.9 parts) was dissolved in absolute ethanol (380 parts) with stirring and was cooled to 20° C. and benzofuranone (100 parts) and 3-methoxybenzaldehyde were added. The reaction mixture was stirred under reflu for 15 minutes and cooled to 20° C. over 1 hour. The reaction mixture was poured into water (900 parts) and the ethanol was removed by evaporation under reduced pressure. Hydrochloric acid was added to the solution until acid and the aqueous phase was decanted to leave a red gum. The gum was dissolved in hot acetic acid (300 parts) and the solution was cooled to 20° C. and a solid was precipitated. The solid was isolated by filtration, washed with ethanol (74 OP) and dried to give 2-(3-methoxyphenyl)-1,3-indandione (55.8 parts) m.pt. 142°-144° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05389597 |
|---|
| Source dataset | uspto-grants-1995_02 |
|---|
| ORD ID | ord-0f752959c2ce469186e19c06d23a269b |
|---|
| Source note | uspto-grants-1995_02 |
|---|