HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 5-(Methylthio)-2-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 5-Chloro-2-nitropyridine | HCID 259806 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(Methylthio)-2-nitropyridine | HCID 22036182 | 45.3% |
Reaction Steps
A methanol (40 mml) solution of 5-chloro-2-nitropyridine (2.0 g. 12.6 mmol) was added dropwise to a methanol (20 ml) solution of sodium thiomethoxide (1.02 g, 13.9 mmol) while being cooled with ice, and after the mixture was stirred for 13 hours while raising its temperature to the room temperature, water added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with water and then with a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. Thereafter, the solvent was distilled off, and the resulting crude product was recrystalized with ethyl acetate-hexane to obtain 972 mg (yield 45%) of 5-methylthio-2-nitropyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414066B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-3f585e1071274f848ebfa24bd15bb4ee |
| Source note | uspto-grants-2008_08 |