HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21638Generated: October 29, 2026
Benzoyl chloride → N-(tert-butyl)benzohydrazide
https://huagongshe.com/reaction/21638
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 | N-(tert-butyl)benzohydrazide | HCID 1275961 | — |
Reaction Steps
To a stirred suspension of t-butylhydrazine hydrochloride (1 g, 0.008M) in toluene (30 ml) at room temperature was added dropwise a 50% aqueous solution of sodium hydroxide (0.64 g, 0.008M). After 15 minutes, the reaction mixture was cooled to 5° C. and a solution of benzoyl chloride (1.12 g, 0.008M) in toluene (5 ml) and a solution of aqueous 50% sodium hydroxide (0.64 g, 0.008M) were added dropwise simultaneously from separate addition funnels while maintaining the temperature at or below 10° C. Following the addition, the reaction mixture was warmed to room temperature and stirred for 1 hour. The reaction was diluted with hexane and the solid N'-t-butyl-N'-benzoylhydrazine was 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-f412726c7f4d4c648d141ddadd2a54cf |
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| Source note | uspto-grants-1995_06 |
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