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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783297Generated: November 3, 2026

Citric Acid → 2-(Cyanomethyl)-5-methylbenzoic acid

https://huagongshe.com/reaction/1783297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
Reactant6-Methyl-2-hydroxyimino-1-indanoneHCID 58717336—
SolventWaterHCID 962—
Product2-(Cyanomethyl)-5-methylbenzoic acidHCID 2308481044.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

6-Methyl-2-hydroxyimino-1-indanone (37 g) and sodium hydroxide (19.7 g) were dissolved in water (287 mL), and p-toluenesulfonyl chloride (44.3 g) was added with stirring at 50° C. After the completion of the reaction, aqueous citric acid solution was added to acidify the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated. Ether was added to the precipitated crystals, and the crystals were collected by filtration to give 2-cyanomethyl-5-methylbenzoic acid (16.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501412B2
Source datasetuspto-grants-2009_03
ORD IDord-8d701be4f7e5458e98f5a8f5e6b675b1
Source noteuspto-grants-2009_03