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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1025421Erstellt: 23. Oktober 2026

Hydrochloric Acid → HCID 178464526, Verbindung

https://huagongshe.com/de/reaction/1025421

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIodoethaneHCID 6340—
EduktPotassium CarbonateHCID 11430—
EduktTetrabutylammonium FluorideHCID 2724141—
EduktHCID 178501248HCID 178501248—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178464526HCID 178464526—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

A mixture of 450 mg of 2-(trimethylsilyl)ethyl 3-{[trans-4-(methoxycarbonyl)cyclohexyl]sulfamoyl}benzoate, 0.15 mL of ethyl iodide, 422 mg of potassium carbonate, and 4.5 mL of DMF was stirred at 65° C. overnight. To the reaction mixture was added water, followed by extraction with ethyl acetate. Then, the organic layer was washed with water and saturated brine in this order, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to obtain a colorless oily substance. To the obtained oily substance were added a solution of tetrabutyl ammonium fluoride (TBAF) in THF (1.0 M, 2.0 mL) and 4.5 mL of THF, followed by stirring at room temperature for 2 hours. To the reaction mixture was added 0.2 M hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was washed with 0.2 M hydrochloric acid, water, and saturated brine in this order, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 355 mg of 3-{ethyl[trans-4-(methoxycarbonyl)cyclohexyl]sulfamoyl}benzoic acid as a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08729068B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-4431d85e244d4e49a8c0b96a036189ad
Quellennotizuspto-grants-2014_05