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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849760Generated: October 27, 2026

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

https://huagongshe.com/reaction/849760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium HydroxideHCID 14798—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductN'-t-butyl-N-cyclohexylcarbonyl-N'-benzoylhydrazineHCID 15294612—

Reaction Conditions

Temperature5 °C

Reaction Steps

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, 0.016 M) 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 hr. 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, 0.008 M) and 50% sodium hydroxide (0.6 g, 0.008M) simultaneously. After addition, the mixture was stirred for 1/2 hr., diluted with hexane and the solid product, N'-t-butyl-N-cyclohexylcarbonyl-N'-benzoylhydrazine, isolated by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06013836
Source datasetuspto-grants-2000_01
ORD IDord-907ad241e45742ceb11fb3a60dda9d88
Source noteuspto-grants-2000_01