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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21632Erstellt: 24. Oktober 2026

Benzoyl chloride → N'-t-butyl-N-cyclohexylcarbonyl-N'-benzoylhydrazine

https://huagongshe.com/de/reaction/21632

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktSodium HydroxideHCID 14798—
EduktCyclohexanecarbonyl chlorideHCID 75938—
Edukttert-Butylhydrazine monohydrochlorideHCID 81889—
LösungsmittelTolueneHCID 1140—
LösungsmittelHexaneHCID 8058—
ProduktN'-t-butyl-N-cyclohexylcarbonyl-N'-benzoylhydrazineHCID 15294612—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

To a stirred suspension of t-butylhydrazine hydrochloride (2.0 g, 0.016M) in toluene (30 ml) was added 50% sodium hydroxide (1.3 g, 0.016M). After 15 minutes, the mixture was cooled to 5° C. and cyclohexanecarbonylchloride (2.4 g, 0.016M) and 50% sodium hydroxide (1.3 g, 0.016M) were added separately and simultaneously so as to maintain the reaction temperature below 10° C. After the addition, the reaction mixture was allowed to warm to room temperature and stirred for 1 hour. The mixture was diluted with hexane and the solid product isolated by filtration. This product (1.5 g, 0.008M) was dissolved in a stirred mixture of toluene (30 ml) and cooled on ice. To this mixture was added benzoylchloride (1.1 g, 0.008M) and 50% sodium hydroxide (0.6 g, 0.008M) simultaneously. After addition, the mixture was stirred for 1/2 hour, diluted with hexane and the solid product, N'-t-butyl-N-cyclohexylcarbonyl-N'-benzoylhydrazine, isolated by filtration.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424333
Quelldatensatzuspto-grants-1995_06
ORD IDord-ea48877fd4e144e58c745cf0f1a5dad6
Quellennotizuspto-grants-1995_06