Benzothiazole-5-carboxylic acid

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Benzothiazole-5-carboxylic acid Basic information
Product Name:Benzothiazole-5-carboxylic acid
Synonyms:1,3-Benzothiazole-5-carboxylic acid;5-Benzothiazolecarboxylicacid(6CI,9CI);Benzothiazole-5-carboxylic acid;1,3-benzothiazole-5-carboxylic acid(SALTDATA: FREE);5-Carboxy-1,3-benzothiazole;5-Benzothiazolecarboxylicacid;Benzothiazole-5-carboxylicaci;benzo[d]thiazole-5-carboxylic acid
CAS:68867-17-4
MF:C8H5NO2S
MW:179.2
EINECS:
Product Categories:BENZOTHIAZOLE;Thiazole
Mol File:68867-17-4.mol
Benzothiazole-5-carboxylic acid Structure
Benzothiazole-5-carboxylic acid Chemical Properties
Melting point 261-262 °C(Solv: water (7732-18-5))
Boiling point 387.7±15.0 °C(Predicted)
density 1.508±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form solid
pka3.57±0.30(Predicted)
color White
InChIInChI=1S/C8H5NO2S/c10-8(11)5-1-2-7-6(3-5)9-4-12-7/h1-4H,(H,10,11)
InChIKeyRBIZQDIIVYJNRS-UHFFFAOYSA-N
SMILESS1C2=CC=C(C(O)=O)C=C2N=C1
Safety Information
WGK Germany WGK 3
HS Code 2934208090
Storage Class11 - Combustible Solids
MSDS Information
Benzothiazole-5-carboxylic acid Usage And Synthesis
Chemical Propertieslight yellow crystal powder
Synthesis
5-Benzothiazolecarboxylicacid,ethylester(6CI,9CI)

103261-70-7

Benzothiazole-5-carboxylic acid

68867-17-4

Ethyl 1,3-benzothiazole-5-carboxylate (5.30 g, 25.6 mmol) was used as a raw material, which was dissolved in a solvent mixture of methanol (150 mL), tetrahydrofuran (40 mL) and water (5 mL). To this solution was added 50% aqueous sodium hydroxide (10 mL). The reaction mixture was stirred at room temperature for 18 hours and then concentrated. The concentrated residue was dispersed in a solvent mixture of water (300 mL) and ether (200 mL), and the organic layer was separated and discarded. Concentrated hydrochloric acid was added to the aqueous layer to adjust the pH to 4, followed by extraction with ethyl acetate (3 x 300 mL). The organic extracts were combined, washed with brine (200 mL), dried over anhydrous sodium sulfate and concentrated to give 4.30 g of benzothiazole-5-carboxylic acid in 94% yield.

References[1] Patent: WO2004/29050, 2004, A1. Location in patent: Page 67
[2] Patent: WO2005/92890, 2005, A2. Location in patent: Page/Page column 70-71
Benzothiazole-5-carboxylic acid Preparation Products And Raw materials
Raw materials5-Benzothiazolecarboxylicacid,ethylester(6CI,9CI)-->Tetrahydrofuran-->Sodium hydroxide-->Water-->Methanol
Preparation Products5-Benzothiazolemethanol(9CI)
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