HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-(Trifluoromethyl)nitrobenzene → HCID 15789206, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-(Trifluoromethyl)nitrobenzene | HCID 7386 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 15789206 | HCID 15789206 | 81% |
Reaction Steps
1.91 g (10 mmol) of 3-nitrobenzotrifluoride, 1.88 g (20 mmol) of 2-aminopyridine and 1.2 g (30 mmol) of sodium hydroxide in the form of microbeads are heated at 50° C. for 6 h in 30 ml of abs. DMSO while passing through dry air. After cooling, the mixture is diluted with ethyl acetate and extracted several times by shaking with water. After drying and stripping off the organic solvent, 3.8 g of crude product are obtained which is purified by chromatography on silica gel using petroleum ether and ethyl acetate (volume ratio 1:1). 2.3 g (8.1 mmol, 81%) of 2-(4-nitro-2-trifluoromethylphenylamino)-pyridine of m.p. 83°-84° C. are thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05612483 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-77e4ab4452b649b79026e5fbba15c348 |
| Source note | uspto-grants-1997_03 |