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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 719760Erstellt: 25. Oktober 2026

Tetrahydrofuran → N-(4-(1-adamantyl)-2-methylphenyl)-2-chloro-5-nitrobenzenesulfonamide

https://huagongshe.com/reaction/719760

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktTriethylamineHCID 8471—
Edukt2-Chloro-5-nitrobenzenesulfonyl chlorideHCID 20630—
Edukt4-(1-Adamantanyl)-2-methylaniline hydrochlorideHCID 16376269—
LösungsmittelWaterHCID 962—
ProduktN-(4-(1-adamantyl)-2-methylphenyl)-2-chloro-5-nitrobenzenesulfonamideHCID 995593136,2%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To 5 mL of a tetrahydrofuran solution comprising 250 mg of 4-(1-adamantyl)-2-methylaniline hydrochloride and 200 mg of triethylamine, 5 mL of a tetrahydrofuran solution comprising 230 mg of 2-chloro-5-nitrobenzenesulfonylchloride was dropwise added, followed by stirring at about 40° C. for about 7 hours. After the mixture was left to stand for cooling, water was added thereto, extraction with chloroform, drying over salt cake and concentration under reduced pressure were carried out to obtain crude crystals. The crude crystals were recrystalized from ether to obtain 150 mg of N-(4-(1-adamantyl)-2-methylphenyl)-2-chloro-5-nitrobenzenesulfonamide (Compound No. 48) having a melting point of 238° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07132546B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-777acafa4f66488789b044b218be0731
Quellennotizuspto-grants-2006_11