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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516480Generated: October 25, 2026

Benzoyl chloride → N'-benzoyl-4-bromobenzohydrazide

https://huagongshe.com/reaction/516480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant4-BromobenzohydrazideHCID 22219—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN'-benzoyl-4-bromobenzohydrazideHCID 378927080%

Reaction Steps

Subsequently, 2.0 g (13.9 mmol) of the 4-bromobenzohydrazide obtained in (i) above was put in a 300-mL three-neck flask, 7 mL of N-methyl-2-pyrrolidone (abbreviation: NMP) was added thereto, and the mixture was stirred. Thereafter, a mixture of 2.5 mL of N-methyl-2-pyrrolidone and 2.5 mL (21.5 mmol) of benzoyl chloride was dripped through a 50-mL dropping funnel, and the mixture was stirred at 80° C. for 3 hours. The obtained solid was washed with water and a sodium carbonate aqueous solution in this order and collected by suction filtration. Then, the solid was recrystallized with acetone; thus, 3.6 g of a white solid of 1-benzoyl-2-(4-bromobenzoyl)hydrazine that was an object was obtained in the yield of 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09112170B2
Source datasetuspto-grants-2015_08
ORD IDord-316e863fba134d848788ff7fb569cca5
Source noteuspto-grants-2015_08