HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851868Generated: October 30, 2026
Hydrochloric Acid → 2-(3-Cyano-4-isobutyloxyphenyl)-1,3-benzothiazole-7-carboxylic acid
https://huagongshe.com/reaction/851868
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 2-(3-cyano-4-isobutyloxyphenyl)-1,3-benzothiazole-carboxylate | HCID 23023851 | — |
| Reactant | Ethanol tetrahydrofuran methanol | HCID 66624091 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3-Cyano-4-isobutyloxyphenyl)-1,3-benzothiazole-7-carboxylic acid | HCID 12132334 | 83% |
Reaction Steps
Methyl 2-(3-cyano-4-isobutyloxyphenyl)-1,3-benzothiazole-carboxylate (288 mg, 0.786 mmol) was dissolved in a mixed solvent (50 mL) of methanol/ethanol/THF (2/1/2), and, then a solution of potassium hydroxide (281 mg, 5 mmol) in water (10 mL) was added and stirred for one hour at room temperature. The mixture was made acidic by addition of aqueous 1M hydrochloric acid, and placed under reduced pressure to distill the solvent off. The residue was extracted with chloroform. The chloroform portion was then dried over anhydrous magnesium sulfate and placed under reduced pressure too distill the solvent off. The residual crystalline product was recrystallized from toluene, to give 230 mg (yield 83%) of the desired compound in the form of a white crystalline product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253154B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-7dabf0aa854348f689c2c225cf01be77 |
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| Source note | uspto-grants-2007_08 |
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