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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
Reactant3-MethoxybenzaldehydeHCID 11569—
Reactant2(3H)-BenzofuranoneHCID 68382—
ReactantSodiumHCID 5360545—
SolventAcetic AcidHCID 176—
Product1H-Indene-1,3(2H)-dione, 2-(3-methoxyphenyl)-HCID 2817810—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389597
Source datasetuspto-grants-1995_02
ORD IDord-0f752959c2ce469186e19c06d23a269b
Source noteuspto-grants-1995_02