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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21635Generated: October 25, 2026

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

https://huagongshe.com/reaction/21635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
Reactant1-Cyclohexenecarbonyl chlorideHCID 142066—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductN'-t-butyl-N-cyclohexenylcarbonyl-N'-benzoylhydrazineHCID 15451994—

Reaction Conditions

Temperature5 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424333
Source datasetuspto-grants-1995_06
ORD IDord-afd9ef446bce4af0b9c4f598804702b2
Source noteuspto-grants-1995_06