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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837463Generated: October 26, 2026

Methyl-3,4,5-trichloro-6-(2-furyl)pyridine-2-carboxylate → Methyl 3,4,5-trichloro-6-(5-chloro-2-furyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/1837463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl-3,4,5-trichloro-6-(2-furyl)pyridine-2-carboxylateHCID 22677507—
ReactantBenyltrimethylammonium tetrachloroiodateHCID 57347110—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
ProductMethyl 3,4,5-trichloro-6-(5-chloro-2-furyl)pyridine-2-carboxylateHCID 2267732051.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784137B2
Source datasetuspto-grants-2004_08
ORD IDord-00e056c2e271435c8505efa59029a4a7
Source noteuspto-grants-2004_08