HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diiodomethane → 2-Iodo-4-methyl-5-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | 2-Amino-4-methyl-5-nitropyridine | HCID 243165 | — |
| Product | 2-Iodo-4-methyl-5-nitropyridine | HCID 23070167 | 28% |
Reaction Steps
To a solution of 4-methyl-5-nitro-2-pyridinamine (12 g, 78.35 mmol) in diiodomethane (100 mL) was added isoamyl nitrite (22 mL, 160.4 mmol) at rt. After stirring for 30 min, the reaction was kept at 80° C. for 2 hr. The reaction was cooled and concentrated; but most of the diiodomethane remained. The crude mixture was loaded into column directly and eluted with 10% of EtOAc in hexane, and 2-iodo-4-methyl-5-nitropyridine (5.7 g, 28%) was obtained as a yellow solid after the removal of solvents under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198456B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-5829d3674d8c46e8b2bcfeb6c671fdd1 |
| Source note | uspto-grants-2012_06 |