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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6958Erstellt: 23. Oktober 2026

Triethylamine → Methyl 5-sulfamoylthiophene-2-carboxylate

https://huagongshe.com/de/reaction/6958

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl AcetateHCID 8857—
Edukt1,3-Bis(diphenylphosphino)propaneHCID 81219—
Edukt5-Bromo-2-thiophenesulfonamideHCID 1241304—
EduktHCID 178418416HCID 178418416—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelMethanolHCID 887—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktMethyl 5-sulfamoylthiophene-2-carboxylateHCID 13425727—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084170B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-7b3ef08a6ec846058fe20b3dbccc2c1d
Quellennotizuspto-grants-2006_08