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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzoic AcidHCID 978—
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product6-Benzothiazolecarboxylic acid, 2-amino-HCID 66740—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344007B2
Source datasetuspto-grants-2013_01
ORD IDord-ea8db082c3824647b8fe800c17c00ca9
Source noteuspto-grants-2013_01