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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837150Generated: November 1, 2026

Benzoyl chloride → HCID 23497778, compound

https://huagongshe.com/reaction/1837150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 191331HCID 191331—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 23497778HCID 23497778—

Reaction Steps

Benzoylchloride (6.33 g, 45 mmol) in pyridine (50 mL) was added over a 15-minute period to a solution of N,N-diethyl-3-(p-nitrophenyl)-propylamine (9.4 g, 45 mmol) in pyridine (50 mL). The solution was refluxed for 1.5 hours. The solvent was evaporated, giving a brown oil. The oil was dissolved in dichloromethane (300 mL) and washed with 1N NaOH (200 mL). The dichloromethane layer was dried and evaporated. Toluene (100 mL) was added to the resulting oil and re-evaporated. The semi-solid residue was washed with pentane, then recrystalized from cyclohexane (125 mL) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780883B2
Source datasetuspto-grants-2004_08
ORD IDord-4d7b3078df9f440d828b9f7f940d2d66
Source noteuspto-grants-2004_08