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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 5-Chloro-2-fluoro-3-nitropyridine | HCID 12275768 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(5-Chloro-3-nitropyridin-2-yl)morpholine | HCID 59631206 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940724B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-947a7104fc6143e9a402bcbce6dcbf96 |
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| Source note | uspto-grants-2015_01 |
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