HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl-3,4,5-trichloro-6-(2-furyl)pyridine-2-carboxylate → Methyl 3,4,5-trichloro-6-(5-chloro-2-furyl)pyridine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl-3,4,5-trichloro-6-(2-furyl)pyridine-2-carboxylate | HCID 22677507 | — |
| Reactant | Benyltrimethylammonium tetrachloroiodate | HCID 57347110 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 3,4,5-trichloro-6-(5-chloro-2-furyl)pyridine-2-carboxylate | HCID 22677320 | 51.5% |
Reaction Steps
Benyltrimethylammonium tetrachloroiodate (292 mg, 0.70 mmol) was added to a solution of methyl-3,4,5-trichloro-6-(2-furyl)pyridine-2-carboxylate (101 mg, 0.33 mmol) in acetic acid (5 mL). After one hour, the suspension was diluted with diethyl ether and the organic mixture was washed with 0.1 N sodium thiosulphate, 0.1 N sodium bicarbonate and dried (MgSO4). The residue was purified by column chromatography (diethyl ether:hexane, 5:95) to give methyl 3,4,5-trichloro-6-(5-chloro-2-furyl)pyridine-2-carboxylate (58 mg, 0.17 mmol): 1H NMR (CDCl3): δ 7.41 (d, J=3.6 Hz, 1H), 6.40 (d, J=3.6 Hz, 1H), 4.05 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06784137B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-00e056c2e271435c8505efa59029a4a7 |
| Source note | uspto-grants-2004_08 |