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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72850Generated: October 25, 2026

1,4-Dichlorobenzene → 4-(2,4-dichlorobenzoyl)-N-acetylpiperidine

https://huagongshe.com/reaction/72850

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DichlorobenzeneHCID 4685—
Reactant1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
Product4-(2,4-dichlorobenzoyl)-N-acetylpiperidineHCID 1307638750%

Reaction Steps

Aluminium chloride (11, 24 g, 84 mmol) is added portionwise to 23 mL of dichlorobenzene (200 mmol). To this suspension 8 g of 1-acetylisonipecotoyl chloride (42 mmol) was added also portionwise. The mixture was stirred 10 minutes at room temperature and then at 90° C. for 4 hours until TLC indicated completion of the reaction that changed from a yellow/orange solution changed into dark orange upon heating. Water was added and the solution was extracted three times with dichloromethane. The combined organic layers were washed with water and brine, dried over magnesium sulfate, filtered and evaporated. The crude product was purified by flash-chromatography on silica gel with hexane:ethyl acetate (1:0 to 0:1) to give 6.3 g (50%) of the product as an orange oil. MS (m/e): 300.2 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829029B2
Source datasetuspto-grants-2014_09
ORD IDord-d08775b157c249249f66914995cf0109
Source noteuspto-grants-2014_09