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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277273Generated: November 1, 2026

Sodium Hydroxide → 6-(4-methylphenyl)-2H-thiochromene-3-carboxylic acid

https://huagongshe.com/reaction/1277273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantethyl 6-(4-methylphenyl)-2H-thiochromene-3-carboxylateHCID 18472236—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
Product6-(4-methylphenyl)-2H-thiochromene-3-carboxylic acidHCID 1847235195%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl 6-(4-methylphenyl)-2H-thiochromene-3-carboxylate (2.12 g, 6.84 mmol) in tetrahydrofuran (20 ml) and acetonitrile (20 ml) was added dropwise 1N sodium hydroxide (7 ml), and the mixture was stirred at 60° C. for 2.5 hours. The solvent was evaporated, and the residue was dissolved in diethylether. The mixture was extracted with water. The organic layer was extracted with 0.5N sodium hydroxide, and both of the aqueous layers were made pH 3 with 6N hydrochloric acid. The mixture was extracted with ethyl acetate, and the organic layer was washed with saturated brine and dried with magnesium sulfate. The solvent was evaporated to give 6-(4-methyl-phenyl)-2H-thiochromene-3-carboxylic acid (1.83 g, 95%) as yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166006
Source datasetuspto-grants-2000_12
ORD IDord-2884af7807d8496c816c6d6e553feb56
Source noteuspto-grants-2000_12