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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dichlorobenzene | HCID 4685 | — |
| Reactant | 1-Acetylpiperidine-4-carbonyl chloride | HCID 100950 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2,4-dichlorobenzoyl)-N-acetylpiperidine | HCID 13076387 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829029B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-d08775b157c249249f66914995cf0109 |
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| Source note | uspto-grants-2014_09 |
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