HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178419731, compound → 2-Bromo-3-nitro-5-(trifluoromethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178419731 | HCID 178419731 | — |
| Reactant | HCID 178526653 | HCID 178526653 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Bromo-3-nitro-5-(trifluoromethyl)pyridine | HCID 46315200 | — |
Reaction Steps
3-Nitro-5-(trifluoromethyl)pyridin-2-ol (31.00 g, 149 mmol) was dissolved in acetonitrile (250 ml) to give a dark brown solution. Phosphorus(V) oxybromide (85 g, 298 mmol) was added and the mixture was heated at reflux for 4.5 hours and then stirred at RT overnight. The reaction mixture was quenched by pouring into vigorously stirring water (600 ml) containing sodium hydrogencarbonate (110 g). The dark brown mixture was extracted with DCM (3×200 ml) and the organic phase was washed with water (200 ml) and brine (100 ml), dried (MgSO4) and concentrated in vacuo to afford the title product as a brown oil. 1H-NMR: [400 MHz, CDCl3, δH, 8.87 (1H, d, J=1.4 Hz, ArH), 8.39 (1H, d, J=1.9 Hz, ArH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476269B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-c3fc454887404730b2acc39214a39a57 |
| Source note | uspto-grants-2013_07 |