HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228286Generated: October 31, 2026
Sodium Hydroxide → 6-(4-methylphenyl)-2H-thiochromene-3-carboxylic acid
https://huagongshe.com/reaction/2228286
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 6-(4-methylphenyl)-2H-thiochromene-3-carboxylate | HCID 18472236 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(4-methylphenyl)-2H-thiochromene-3-carboxylic acid | HCID 18472351 | 95% |
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-methylphenyl)-2H-thiochromene-3-carboxylic acid (1.83 g, 95%) as yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413947B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-b570e3daf00a4bd7877df3bd7a655d32 |
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| Source note | uspto-grants-2002_07 |
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