HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197247Generated: October 31, 2026
Benzoyl chloride → 1,2-Dibenzoyl-1-(tert-butyl)hydrazine
https://huagongshe.com/reaction/1197247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,2-Dibenzoyl-1-(tert-butyl)hydrazine | HCID 86307 | — |
Reaction Steps
To a stirred suspension of t-butylhydrazine hydrochloride (1.24 g, 10 mmoles) in toluene (50 ml) at room temperature, was added dropwise a solution of 50% aqueous sodium hydroxide (0.8 g, 10 ml). After 15 minutes, the reaction mixture was cooled to 5° C. and solutions of benzoyl chloride (2.82 gm, 20 ml) in toluene (7 ml) and 50% aqueous sodium hydroxide (1.6 g) were added dropwise and simultaneously from separate addition funnels while maintaining the temperature below 10° C. Following the addition, the reaction mixture was warmed to room temperature and stirred for 1 hr. The reaction mixture was diluted with ether and the product isolated by filtration. The product was washed with water and ether and dried. The product was recrystallized from ethermethanol to afford N'-t-butyl-N,N'-dibenzoylhydrazine as a white powder: m.p. 174°-176° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05117057 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-330e5c8895f34e13af3dd980be2d8416 |
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| Source note | uspto-grants-1992_05 |
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