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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189272Generated: October 30, 2026

Acetyl chloride → 1-[4-(4-Nitrophenyl)-1-piperidinyl]ethanone

https://huagongshe.com/reaction/2189272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(4-Nitrophenyl)piperidineHCID 15925817—
SolventDichloromethaneHCID 6344—
Product1-[4-(4-Nitrophenyl)-1-piperidinyl]ethanoneHCID 58015948110%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(4-Nitro-phenyl)-piperidin (206 mg, 1 mmol) in CH2Cl2 (3 mL) is added AcCl (0.106 mL, 1.5 mmol) at 0° C. Then Et3N (0.253 mL, 1.8 mmol) is added slowly. The mixture is stirred at 0° C. for 10 minutes. Then saturated NaHCO3 aqueous solution is added. The aqueous layer is extracted with CH2Cl2, and the organic extracts are dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product is purified by column chromatography (SiO2, MeOH:CH2Cl2=0.7:99.3 to 6:93) to give 273 mg of the title compound as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324225B2
Source datasetuspto-grants-2012_12
ORD IDord-329d257e9d614ed5885aa7661ba30e77
Source noteuspto-grants-2012_12