HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21632Generated: October 26, 2026
Benzoyl chloride → N'-t-butyl-N-cyclohexylcarbonyl-N'-benzoylhydrazine
https://huagongshe.com/reaction/21632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N'-t-butyl-N-cyclohexylcarbonyl-N'-benzoylhydrazine | HCID 15294612 | — |
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, 0.016M) 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05424333 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-ea48877fd4e144e58c745cf0f1a5dad6 |
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| Source note | uspto-grants-1995_06 |
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