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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377761Generated: October 25, 2026

4-(Methylsulfonyl)benzaldehyde → HCID 70286603, compound

https://huagongshe.com/reaction/377761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methylsulfonyl)benzaldehydeHCID 220376—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 5-methoxy-2-methyl-3-indenylacetateHCID 53634864—
SolventWaterHCID 962—
ProductHCID 70286603HCID 70286603—

Reaction Steps

25% methanolic sodium methoxide (16 ml, 2.0 equivalents) is treated with a solution of methyl 5-methoxy-2-methyl-3-indenylacetate (from Example 4, Part C) (8.7 g; 0.037 mol) and p-methylsulfonylbenzaldehyde, (6.3 g; 1.1 equivalent). The mixture is stirred at reflux under nitrogen for 2 hours. An equal volume of water is added slowly, and refluxing is continued for 30 min. The solution is cooled, is diluted with water and is washed with ether. Residual ether is blown off with nitrogen. The aqueous solution is acidified with 10% hydrochloric acid. The precipitated product is collected and is washed thoroughly with water. The crude product is crystallized from methanol to give (Z)-5-methoxy-2-methyl-1-(p-methylsulfonylbenzylidene)-3-indenylacetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028116
Source datasetuspto-grants-2000_02
ORD IDord-113586e271734fa8a1342d6dff985c0c
Source noteuspto-grants-2000_02