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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6958Generated: October 27, 2026

Triethylamine → Methyl 5-sulfamoylthiophene-2-carboxylate

https://huagongshe.com/reaction/6958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
Reactant5-Bromo-2-thiophenesulfonamideHCID 1241304—
ReactantHCID 178418416HCID 178418416—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 5-sulfamoylthiophene-2-carboxylateHCID 13425727—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-bromothiophene-2-sulfonamide (0.50 g, 2.1 mmol), triethyl amine (1 mL), methanol (1 mL), palladium acetate (0.046 g, 2.1 mmol) and 1,3-bis(diphenylphosphino) propane (0.085 g, 2.1 mmol) (addition in that order) in dimethylformamide (5 mL, anhydrous) is saturated with carbon monoxide gas, at room temperature. This reaction mixture is heated to 100° C. and stirred overnight, under a carbon monoxide atmosphere. 10 mL of brine and 10 mL of ethyl acetate are added to the reaction mixture. The organic phase is separated and the aqueous layer is extracted with 10 mL ethyl acetate. The combined organic layers are dried over sodium sulfate, concentrated in vacuo, and then chromatographed on silica (0–1% methyl alcohol in methylene chloride) to give the title compound, as a yellow solid (0.15 g, 34% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084170B2
Source datasetuspto-grants-2006_08
ORD IDord-7b3ef08a6ec846058fe20b3dbccc2c1d
Source noteuspto-grants-2006_08