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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74182Generated: October 23, 2026

Ethanol → 5-Bromo-2-(tetrahydropyran-4-yl)nitrobenzene

https://huagongshe.com/en/reaction/74182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
Reactant4-AminotetrahydropyranHCID 419223—
Reactant4-Bromo-1-fluoro-2-nitrobenzeneHCID 2736328—
SolventWaterHCID 962—
Product5-Bromo-2-(tetrahydropyran-4-yl)nitrobenzeneHCID 6749882691.2%

Reaction Steps

An eggplant flask was charged with 5-bromo-2-fluoronitrobenzene (3.0 g, 13.6 mmol), triethylamine (1.66 g, 16.3 mmol), 4-aminotetrahydropyran (1.52 g, 15.0 mmol), and ethanol (60 mL), and this was heated to reflux with stirring for 2 hours. After concentration of the reaction mixture under reduced pressure, water (60 mL) was added and this was stirred as is at room temperature for 30 minutes. The precipitated crystals were filtered off and washed with water. The crystals obtained were dried at reduced pressure with heating to yield the title compound (3.55 g, 86% yield) as a reddish-orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-3a8229f9c17741f3846e907f5ce44fc5
Source noteuspto-grants-2014_09