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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 352172Erstellt: 24. Oktober 2026

Benzenesulfonyl chloride → (3-Aminocyclohexyl)(phenylsulfonyl)amine

https://huagongshe.com/de/reaction/352172

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenesulfonyl chlorideHCID 7369—
EduktSodium HydroxideHCID 14798—
Edukt1,3-CyclohexanediamineHCID 18814—
LösungsmittelDichloromethaneHCID 6344—
Produkt(3-Aminocyclohexyl)(phenylsulfonyl)amineHCID 22714123—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 1,3-diaminocyclohexane (1.14 g, 10 mmol, undetermined isomer mixture) in methylene chloride (50 mL) was cooled to 0° C. and phenylsulfonyl chloride (0.64 mL, 5 mmol) was added dropwise. The mixture was stirred at 0° C. for 4 h, then 1N sodium hydroxide solution (10 mL) was added and the mixture stirred an additional 5 min. The phases were separated, the organic phase was dried (K2CO3), filtered, and concentrated in vacuo. Toluene was added and the mixture re-concentrated to remove any remaining diamine, to give 0.77 g of a semi solid. 1H—NMR was consistent with the desired structure. MS (ion spray) 255 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743794B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-00c7fddcef0447a38fcc09444aa75ea4
Quellennotizuspto-grants-2004_06