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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093175Generated: November 1, 2026

Iodine → Benzyl 5-(3-iodo-4-methoxyphenyl)-6-methylpyridine-2-carboxylate

https://huagongshe.com/reaction/2093175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBenzyl 5-(4-methoxyphenyl)-6-methylpyridine-2-carboxylateHCID 57704814—
CatalystHCID 178418844HCID 178418844—
SolventMethanolHCID 887—
ProductBenzyl 5-(3-iodo-4-methoxyphenyl)-6-methylpyridine-2-carboxylateHCID 57704790—

Reaction Steps

Benzyl 5-(4-methoxyphenyl)-6-methylpyridine-2-carboxylate (150 mg, 0.45 mmol), iodine (228 mg, 0.898 mmol), silver sulfate (402 mg, 1.29 mmol) were stirred in methanol (3 mL) at room temperature overnight. More iodine (57 mg, 0.22 mmol) and silver sulfate (100 mg, 0.32 mmol) were added into reaction mixture after 25 hours. Added aqueous NaHSO3 solution (sat., 20 mL) into the reaction mixture after additional 1.5 hours to quench the reaction. The reaction mixture was extracted with ethyl acetate. The combined extracts were dried over Na2SO4 followed by filtration and concentration to afford a clear oil. The crude oil was purified by preparative TLC on SiO2 (eluted with 30% ethyl acetate in hexanes) to afford benzyl 5-(3-iodo-4-methoxyphenyl)-6-methylpyridine-2-carboxylate. LCMS calc.=459.03; found=460.17 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440702B2
Source datasetuspto-grants-2013_05
ORD IDord-829039ceeee2476593f9029e418d737d
Source noteuspto-grants-2013_05