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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749630Generated: October 26, 2026

Benzoyl chloride → Benzanilide

https://huagongshe.com/reaction/749630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantDiphenylamineHCID 11487—
SolventPyridineHCID 1049—
ProductBenzanilideHCID 7168230.7%

Reaction Steps

830 mg (2.44 mmole) of the aniline compound obtained in step 1 was dissolved in 10 mL of pyridine, 0.340 mL (2.93 mmoles) of benzoylchloride was added, and the mixture was stirred overnight at room temperature. When the reaction had ended, the solvent was removed under reduced pressure. Ethyl acetate and 1N HCl aqueous solution were added to the residue. The mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine and dried with anhydrous sodium sulfate. The solvent was removed under reduced pressure, yielding 1.11 g of N-benzoylaniline compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402696B2
Source datasetuspto-grants-2008_07
ORD IDord-bd63148fe211469f996a363c66a2399c
Source noteuspto-grants-2008_07