HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923422Generated: October 26, 2026
Benzoyl chloride → N'-benzoyl-4-bromobenzohydrazide
https://huagongshe.com/reaction/1923422
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 4-Bromobenzohydrazide | HCID 22219 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N'-benzoyl-4-bromobenzohydrazide | HCID 3789270 | — |
Reaction Steps
2.0 g (13.9 mmol) of 4-bromobenzoylhydrazine was put into a 300 mL three-neck flask, 7 mL of N-methyl-2-pyrrolidone was added thereto, and the mixture was stirred at a room temperature. A mixed solution of 5.0 mL of N-methyl-2-pyrrolidone and 2.5 mL (21.5 mmol) of benzoyl chloride was dripped into the solution through a 50 mL dropping funnel. The mixture was stirred at 80° C. for 3 hours. After the reaction, a solid was precipitated out with the addition of the reactive mixture to approximately 200 mL of water. The precipitated solid was collected by suction filtration. The collected solid was washed with water, a saturated sodium hydrogen carbonate solution, and saturated saline, in the order given. The obtained solid was recrystallized with a mixed solvent of acetate and hexane, so that 3.6 g of a white solid, which was the object of the synthesis, was obtained at a yield of 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178217B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-86907efb76494f02a9e160e1576d732b |
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| Source note | uspto-grants-2012_05 |
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