HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454896Generated: October 30, 2026
Morpholine → 4-(2-Fluoropyridin-3-yl)morpholine
https://huagongshe.com/reaction/454896
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2-Fluoro-3-iodopyridine | HCID 7009501 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | 4-(2-Fluoropyridin-3-yl)morpholine | HCID 58547698 | 67.5% |
Reaction Steps
A microwave reaction vessel was charged with 2-fluoro-3-iodopyridine (purchased from Maybridge™) (0.565 g, 2.53 mmol), morpholine (purchased from Aldrich™) (0.221 ml, 2.53 mmol), Pd2(dba)3 (purchased from Strem™) (0.154 g, 0.152 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (purchased from Strem™) (0.135 g, 0.304 mmol), and sodium t-butoxide (0.8 g, 7.6 mmol). The reaction mixture was stirred and heated in a Discover® model microwave reactor (CEM, Matthews, N.C.) at 150° C. for 20 min (125 watts, Powermax feature on, ramp time 5 min). Solvent was evaporated. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Biotage pre-packed silica gel column, eluting with a gradient of 1% to 5% MeOH in CH2Cl2, to provide 4-(2-fluoropyridin-3-yl)morpholine (0.311 g, 67.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497265B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-2e7079a4ce79493f8112aba0c85e0dbc |
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| Source note | uspto-grants-2013_07 |
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