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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188237Generated: October 29, 2026

2-Aminothiophenol → 2-(4-Bromophenyl)benzothiazole

https://huagongshe.com/reaction/2188237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
Reactant4-Bromobenzoic acidHCID 11464—
ReactantPhosphorus trichlorideHCID 24387—
ReactantSodium BicarbonateHCID 516892—
SolventTolueneHCID 1140—
Product2-(4-Bromophenyl)benzothiazoleHCID 232060227.9%

Reaction Steps

A solution of 15.0 g of 4-bromobenzoic acid (74 mmol) and 13.9 g of 2-aminothiophenol (110 mmol) in 250 mL of dry toluene was heated to 45° C. and 10.1 mL of phosphorus trichloride (110 mmol) was slowly added to the reaction mixture via syringe. The mixture was allowed to reflux for 4 h. The reaction mixture was cooled to room temperature, filtered and the filtrate was concentrated under reduced pressure to afford a yellow solid. The solid was slowly added to 500 mL of saturated aq. NaHCO3 and the aqueous solution was extracted with 2×200 mL of ethyl acetate. The combined organic solutions were washed with water (3x), dried over sodium sulfate and concentrated to dryness. The crude product was purified by column chromatography to afford 6.0 g of 2-(4-bromophenyl)benzothiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410732B2
Source datasetuspto-grants-2002_06
ORD IDord-b26fab538f844630a0a50e4fe6cf0677
Source noteuspto-grants-2002_06