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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971939Generated: October 28, 2026

1-Indanone → 1H-Inden-1-one, 2-[[4-(diethylamino)-2-methylphenyl]methylene]-2,3-dihydro-

https://huagongshe.com/reaction/971939

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IndanoneHCID 6735—
ReactantSodium HydroxideHCID 14798—
ReactantBenzaldehyde, 4-(diethylamino)-2-methyl-HCID 66695—
SolventEthanolHCID 702—
Product1H-Inden-1-one, 2-[[4-(diethylamino)-2-methylphenyl]methylene]-2,3-dihydro-HCID 5424770680.1%

Reaction Conditions

Temperature5 °C

Reaction Steps

A solution of 50 g. (0.3785 mole) 1-indanone and 77.75 g. of 93% 4-diethylamino-2-methylbenzaldehyde in 150 ml. of ethanol was stirred and 94 ml. of a solution of warm (approx. 30° C.) 25% aqueous sodium hydroxide was added. This reaction mixture was heated to reflux for 45 minutes. A solid precipitate began appearing after 30 minutes. Next, the mixture was cooled to about 5° C. and the precipitate filtered and washed with petroleum ether. After air drying, the resulting solid was washed with water until the wash material was pH 7.0. The washed precipitate was recrystallized from 80% aqueous ethanol to yield 92.6 g. (80.1% yield) of 2-(4'-diethylamino-2'-methylbenzylidene)-1-indanone (m.p. 133.5°-134.5° C.), U.V. spectra and ε values are set forth in Table 3 below. The structure was confirmed by both infrared and nuclear magnetic resonance spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04162162
Source datasetuspto-grants-1979_07
ORD IDord-4b336c75c7b24f33ad01e7c3128a6d5e
Source noteuspto-grants-1979_07