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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876914Generated: November 2, 2026

Iodine → Methyl 5-iodothiophene-2-carboxylate

https://huagongshe.com/reaction/1876914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium ThiosulfateHCID 24477—
ReactantMethyl thenoateHCID 79340—
ReactantBis(trifluoroacetoxy)iodobenzeneHCID 102317—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-iodothiophene-2-carboxylateHCID 1315639990.5%

Reaction Steps

To a stirred solution of methyl thiophene-2-carboxylate (0.46 mL, 4 mmol) in anhydrous methylene chloride (5 mL) was added iodine (510 mg, 2 mmol) followed by [bis(trifluoroacetoxy)iodo]benzene (900 mg, 2.1 mmol). The reaction mixture was stirred at RT for 1.5 hr before saturated aqueous sodium bicarbonate solution (10 mL) and saturated aqueous sodium thiosulfate solution (2 mL) were added. The mixture was then stirred at RT for 20 min. The aqueous layer was separated and extracted with methylene chloride (2×1 mL). The combined organic solutions were dried (Na2SO4). Silica gel flash chromatography (0-100% ethyl acetate in hexanes) gave methyl 5-iodothiophene-2-carboxylate (500 mg, 1.9 mmol, 47% yield) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309730B2
Source datasetuspto-grants-2012_11
ORD IDord-1bf6ee4dc11545b6be1b5670c83ac4fa
Source noteuspto-grants-2012_11