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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74157Generated: October 23, 2026

Hydrochloric Acid → 4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acid

https://huagongshe.com/en/reaction/74157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant4-Fluoro-3-nitrobenzoic acidHCID 67987—
Reactant4-AminotetrahydropyranHCID 419223—
ReactantOxan-2-amineHCID 14471248—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acidHCID 43610332101.2%

Reaction Steps

4-Fluoro-3-nitrobenzoic acid (126.4 g, 0.68 mol) was dissolved in ethanol (880 mL). Triethylamine (82.6 g, 0.82 mol), 4-aminotetrahydropyran (82.7 g, 0.81 mol) were added in turn dropwise, and after the additions the reaction solution was heated to reflux. After refluxing for 5 h, triethylamine (8.3 g, 82 mmol), aminotetrahydropyran (8.3 g, 81 mmol) were added, and this was refluxed for a further 9 hours. After the reaction mixture was allowed to cool to room temperature, 2N HCl (880 mL) and water (880 mL) were added and after stirring for awhile, the solid obtained was filtered off. This was forced air-dried at 60° C. to yield the title compound (183.3 g, quant.) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-3d585bfc7faf417584411f9094ad5215
Source noteuspto-grants-2014_09