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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21635Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/21635

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktSodium HydroxideHCID 14798—
Edukttert-Butylhydrazine monohydrochlorideHCID 81889—
Edukt1-Cyclohexenecarbonyl chlorideHCID 142066—
LösungsmittelTolueneHCID 1140—
LösungsmittelHexaneHCID 8058—
ProduktN'-t-butyl-N-cyclohexenylcarbonyl-N'-benzoylhydrazineHCID 15451994—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

To a stirred suspension of t-butylhydrazine hydrochloride (0.86 g, 0.007M) in toluene (30 ml) was added 50% sodium hydroxide (0.55 g, 0.007M). After 15 minutes, the mixture was cooled to 5° C. and cyclohexenylcarbonyl chloride (1.0 g, 0.007M) and 50% sodium hydroxide (0.55 g, 0.007M) 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 (1.2 g, 0.006M) was dissolved in toluene (30 ml) and cooled on ice while stirring. To this mixture was added benzoylchloride (1.0 g, 0.007M) and 50% sodium hydroxide (1.3 g, 0.007M) simultaneously. After addition, the mixture was stirred for 1/2 hour, diluted with hexane and the solid product, N'-t-butyl-N-cyclohexenylcarbonyl-N'-benzoylhydrazine, was isolated by filtration.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424333
Quelldatensatzuspto-grants-1995_06
ORD IDord-afd9ef446bce4af0b9c4f598804702b2
Quellennotizuspto-grants-1995_06