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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427292Generated: November 1, 2026

4-Nitrophenol → Methoxy-2-trifluoromethylbenzothiazole-7-carboxylic acid 4-nitrophenyl ester

https://huagongshe.com/reaction/427292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-Methoxy-2-trifluoromethylbenzothiazole-7-carboxylic acidHCID 18356995—
SolventDichloromethaneHCID 6344—
ProductMethoxy-2-trifluoromethylbenzothiazole-7-carboxylic acid 4-nitrophenyl esterHCID 6968966074.6%

Reaction Steps

A suspension of 4-methoxy-2-trifluoromethylbenzothiazole-7-carboxylic acid (140 mg) in dichloromethane (10ml) was treated with p-nitrophenol (72 mg), dimethylaminopyridine (catalytic) and 1-(3-dimethylaminopropyl)-3-ethyl carbodimide hydrochloride (150 mg). The mixture was stirred at room temperature for 12 hours and the reaction washed with water (10 ml). The organic layer was separated, dried over magnesium sulphate (5 g) and evaporated in vacuo. Purification by flash chromatography (eluent 50% ethyl acetate/hexane) yielded the title compound as an off-white solid (150 mg). TLC Rf 0.13 (50% ethyl acetate in heptane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313116B1
Source datasetuspto-grants-2001_11
ORD IDord-4a57574299c14853ba29b6f739adcca7
Source noteuspto-grants-2001_11