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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzoyl chloride | HCID 7412 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Edukt | 1-Cyclohexenecarbonyl chloride | HCID 142066 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | N'-t-butyl-N-cyclohexenylcarbonyl-N'-benzoylhydrazine | HCID 15451994 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05424333 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-afd9ef446bce4af0b9c4f598804702b2 |
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| Quellennotiz | uspto-grants-1995_06 |
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