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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264110Generated: October 30, 2026

4-Nitrobenzoyl chloride → 2-(4-Nitrophenyl)Benzo[D]Thiazole

https://huagongshe.com/reaction/2264110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant2-AminothiophenolHCID 8713—
SolventBenzeneHCID 241—
Product2-(4-Nitrophenyl)Benzo[D]ThiazoleHCID 82750073.2%

Reaction Steps

A solution of 4-nitrobenzoyl chloride (1.49 g, 8.0 mmol) in benzene (anhydrous, 10 mL) was added dropwise to 2-aminothiophenol (1.0 g, 8.0 mmol in 10 ml of benzene) at room temperature. The reaction mixture was allowed to stir for 16 hr. The reaction was quenched with water (20 mL). The aqueous layer was separated and extracted with ethyl acetate (3×10 ml). The combined organic layers were dried and evaporated. The crude product was purified with flush column, (hexane:ethyl acetate=85:15) to give 1.5 g (73.2%) of product as light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07854920B2
Source datasetuspto-grants-2010_12
ORD IDord-1ce233ea3ffd41108572060eabe8dda0
Source noteuspto-grants-2010_12