Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431378Generated: November 3, 2026

Morpholine → 4-(5-Chloro-3-nitropyridin-2-yl)morpholine

https://huagongshe.com/reaction/1431378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant5-Chloro-2-fluoro-3-nitropyridineHCID 12275768—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-(5-Chloro-3-nitropyridin-2-yl)morpholineHCID 59631206—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 5-chloro-2-fluoro-3-nitropyridine (5 g, 28 mmol) in THF (40 mL) was added morpholine (4 mL, 42 mmol). The reaction was stirred at 0° C. for ten min, at rt for 1 h, and refluxed for four h. The reaction was then cooled to rt, taken up in EtOAc, and washed with satd aq. sodium bicarbonate and brine. The organic layer was dried (magnesium sulfate) and concentrated, affording 4-(5-chloro-3-nitropyridin-2-yl)morpholine as a yellow oil. Mass Spectrum (ESI) m/e=244.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-947a7104fc6143e9a402bcbce6dcbf96
Source noteuspto-grants-2015_01