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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402433Generated: October 31, 2026

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

https://huagongshe.com/reaction/2402433

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 numberUS08796314B2
Source datasetuspto-grants-2014_08
ORD IDord-3d20fdc2805b4d2f9a68d98c0d9b74c4
Source noteuspto-grants-2014_08