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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129674Erstellt: 25. Oktober 2026

Tetrahydrofuran → 4-[3-(1-Adamantyl)-4-methoxybenzoyloxy]benzenesulfonamide

https://huagongshe.com/reaction/129674

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktDicyclohexylcarbodiimideHCID 10868—
Eduktp-HydroxybenzenesulfonamideHCID 74093—
Edukt3-(1-Adamantyl)-4-methoxybenzoic acidHCID 5296503—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelWaterHCID 962—
Produkt4-[3-(1-Adamantyl)-4-methoxybenzoyloxy]benzenesulfonamideHCID 1485250946%

Reaktionsschritte

Into a round bottom flask, there are introduced 2.86 g (10 mmoles) of 3-(1-adamantyl)-4-methoxybenzoic acid, 1.73 g (10 mmoles) of 4-hydroxybenzenesulfonamide and 50 ml of THF. There are added, successively, 2.1 g (10 mmoles) of 1,3-dicyclohexylcarbodiimide and then 1.22 (10 mmoles) of 4-dimethylaminopyridine. The medium is stirred at ambient temperature for 4 hours. The reaction medium is poured into water and extracted with ethyl ether. The organic phase is decanted, washed with water, dried on magnesium sulfate and evaporated. The resulting solid is purified by chromatography on a silica column eluted by a 60:40 mixture of ethyl ether and hexane. After evaporation of the solvents, 2 g (46% yield) of 4-[3-(1-adamantyl)-4-methoxybenzoyloxy]benzenesulfonamide having a melting point of 223°-224° C. are recovered.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05468897
Quelldatensatzuspto-grants-1995_11
ORD IDord-adfbc46c6fca49afa2549a254fac1eb5
Quellennotizuspto-grants-1995_11