HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798992Generated: October 30, 2026
4-Aminobenzoic Acid → 6-Benzothiazolecarboxylic acid, 2-amino-
https://huagongshe.com/reaction/1798992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobenzoic Acid | HCID 978 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Benzothiazolecarboxylic acid, 2-amino- | HCID 66740 | — |
Reaction Steps
A solution of 4-aminobenzoic acid (1.37 g, 14 mmol) in AcOH (16 mL) may be added with potassium thiocyanate (3.9 g, 40 mmol) and may be stirred for 15 minutes. A solution of bromine (0.5 mL, 10 mmol) in AcOH (6 mL) may then be added slowly into the reaction mixture in water bath, where the temperature may be maintained at about 25° C. The resulting mixture may be stirred overnight. The mixture may then be filtered, and the pale yellow precipitate may then be further recrystallized with the minimal volume of aqueous hydrochloric acid (6 M). A pale yellow product of formula (2) may be collected with the following characterization: 1H NMR (CD3OD, 500 MHz): δ 4.96 (2H, brs), 7.58 (1H, d, J=8.0 Hz), 8.14 (1H, dd, J=8.5 Hz and 1.5 Hz), 8.47-8.47 (1H, m); 13C NMR (CDCl3): δ 12.1, 23.7, 54.6, 85.0, 85.1, 122.5, 123.9, 127.9, 128.3, 132.7, 151.9, 155.3, 168.0, 178.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344007B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-ea8db082c3824647b8fe800c17c00ca9 |
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| Source note | uspto-grants-2013_01 |
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