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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923422Generated: October 26, 2026

Benzoyl chloride → N'-benzoyl-4-bromobenzohydrazide

https://huagongshe.com/reaction/1923422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant4-BromobenzohydrazideHCID 22219—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN'-benzoyl-4-bromobenzohydrazideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178217B2
Source datasetuspto-grants-2012_05
ORD IDord-86907efb76494f02a9e160e1576d732b
Source noteuspto-grants-2012_05