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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1925707Erstellt: 24. Oktober 2026

Methyl 3-amino-2-thiophenecarboxylate → Methyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylate

https://huagongshe.com/de/reaction/1925707

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
Edukt4-t-Butylbenzenesulfonyl chlorideHCID 139882—
LösungsmittelPyridineHCID 1049—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylateHCID 801564366%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To a solution of methyl 3-aminothiophene-2-carboxylate (0.55 g; 3.5 mmol) in pyridine (2 mL) and dichloromethane (2 mL) was added 4-tert-butylbenzenesulfonyl chloride (0.98 g; 4.2 mmol). The resulting mixture was warmed to 40° C. to aid in solubility, then stirred at room temperature for 48 hours. The reaction mixture was diluted with dichloromethane and washed with aqueous hydrochloric acid (2N). The aqueous layer was separated and extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, decanted, and filtered through a and of silica. The silica was washed with dichloromethane. The eluant was combined with hexanes and allowed to stand. After 24 hours the resulting solid product was collected by filtration to give the desired product as a white solid (817 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08178699B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-4fc1342cfdfe4611b700d4c23e1bcb89
Quellennotizuspto-grants-2012_05