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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 926045Erstellt: 24. Oktober 2026

Citric Acid → Methyl 2-{[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}benzoate

https://huagongshe.com/de/reaction/926045

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCitric AcidHCID 311—
EduktDichloromethaneHCID 6344—
EduktMethyl AnthranilateHCID 8635—
Edukt2-(Trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoateHCID 86676334—
LösungsmittelPyridineHCID 1049—
ProduktMethyl 2-{[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}benzoateHCID 7123867992,2%

Reaktionsschritte

To a mixture of 2.09 g of 2-(trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoate and 20 mL of methylene chloride were added 982 mg of methyl 2-aminobenzoate and 2.10 mL of pyridine under ice-cooling, followed by stirring at room temperature for 15 hours. To the reaction mixture was added a 10% aqueous citric acid solution, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 2.61 g of methyl 2-{[(3-{[2-(trimethylsilyl)ethoxy]carbonyl}phenyl)sulfonyl]amino}benzoate as a colorless oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09284295B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-85f77c7d02fa4c4e97559078b7e23ae5
Quellennotizuspto-grants-2016_03