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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 849763Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/849763

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 hr. 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 hr., diluted with hexane and the solid product, N'-t-butyl-N-cyclohexenylcarbonyl-N'-benzoylhydrazine, isolated by filtration.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06013836
Quelldatensatzuspto-grants-2000_01
ORD IDord-6d5ca1b9f4054febacf23bda7f174b4b
Quellennotizuspto-grants-2000_01