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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 2-(3-cyano-4-isobutyloxyphenyl)-1,3-benzothiazole-carboxylateHCID 23023851—
ReactantEthanol tetrahydrofuran methanolHCID 66624091—
SolventWaterHCID 962—
Product2-(3-Cyano-4-isobutyloxyphenyl)-1,3-benzothiazole-7-carboxylic acidHCID 1213233483%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253154B2
Source datasetuspto-grants-2007_08
ORD IDord-7dabf0aa854348f689c2c225cf01be77
Source noteuspto-grants-2007_08