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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916516Generated: November 1, 2026

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

https://huagongshe.com/reaction/916516

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 numberUS07270800B2
Source datasetuspto-grants-2007_09
ORD IDord-847a8b1bb1034d89a9258a45ea828d68
Source noteuspto-grants-2007_09