HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiomorpholine → 4-(5-Nitro-2-pyridinyl)thiomorpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiomorpholine | HCID 67164 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(5-Nitro-2-pyridinyl)thiomorpholine | HCID 2798452 | — |
Reaction Steps
To a solution of 20 g (126 mmol) of 2-chloro-5-nitropyridine in 200 ml tetrahydrofuran were added dropwise 32.5 ml (315 mmol) thiomorpholine within 10 min. The reaction mixture was refluxed for additional 2 h. After cooling to room temperature, the solvent was removed in vacuo and the residue was re-dissolved in 200 ml ethyl acetate. The organic phase was washed with 200 ml 1 N sodium bicarbonate solution, dried (magnesium sulfate) and evaporated to give 29.3 g (quantitative) of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06849624B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-0a6d260271f0483bbbb1796c2958fed9 |
| Source note | uspto-grants-2005_02 |