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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282106Generated: November 1, 2026

Potassium Carbonate → Ethyl 4-cyano-3-iodo-5-(methylsulfonyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/2282106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium SulfiteHCID 24437—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantEthyl 4-cyano-3-iodo-5-(methylthio)thiophene-2-carboxylateHCID 40152061—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-cyano-3-iodo-5-(methylsulfonyl)thiophene-2-carboxylateHCID 4015206286.5%

Reaction Steps

Ethyl 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylate (7.2 g, 20.4 mmol) was dissolved in DCM (200 mL) and THF (100 mL) and m-CPBA (9.14 g, 40.8 mmol) was added. The reaction mixture was stirred at rt overnight. Sodium sulfite (5.14 g, 40.8 mmol) was added, stirred for 10 minutes followed by addition of potassium carbonate (8.45, 61.2 mmol). The suspension was stirred at rt for 1 hour and filtered through celite, washed with DCM and the solvent was evaporated to afford ethyl 3-iodo-4-cyano-5-(methylsulfonyl)thiophene-2-carboxylate (6.80 g, 78%). LCMS: (FA) ES+ 386. 1H NMR (400 MHz, d1-chloroform) δ: 4.45 (q, 2H), 3.38 (s, 3H), 1.43 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139589B2
Source datasetuspto-grants-2015_09
ORD IDord-f05113747b244bbc8d6b00ab23280c19
Source noteuspto-grants-2015_09