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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377758Generated: October 26, 2026

4-(Methylsulfonyl)benzaldehyde → (Z)-1-(p-methylsulfonylbenzylidene)-5-dimethylamino-2-methyl-3-indenylacetic acid

https://huagongshe.com/reaction/377758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methylsulfonyl)benzaldehydeHCID 220376—
ReactantMethyl 5-dimethylamino-2-methyl-3-indenylacetateHCID 22456970—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(Z)-1-(p-methylsulfonylbenzylidene)-5-dimethylamino-2-methyl-3-indenylacetic acidHCID 70288307—

Reaction Steps

p-Methylsulfonylbenzaldehyde (1.5 g) is added to a solution of methyl 5-dimethylamino-2-methyl-3-indenylacetate (2.5 g) from Example 3 Part B in 1,2-dimethoxyethane (1.5 ml) at 0° C. followed by the addition of potassium t-butoxide (1.1 g). The reaction mixture is kept in the ice-bath for 4 hours and at room temperature for 18 hours. The mixture is diluted with ether (15 ml), and the potassium salt is filtered off. The salt is dissolved in 30 ml of water and neutralized with dilute hydrochloric acid to pH 6-6.5. The crude acid precipitates, is collected by filtration and is recrystallized to give pure (Z)-1-(p-methylsulfonylbenzylidene)-5-dimethylamino-2-methyl-3-indenylacetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028116
Source datasetuspto-grants-2000_02
ORD IDord-5986da5bcbb94caca87cddaa171c9d2b
Source noteuspto-grants-2000_02