HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982497Generated: October 30, 2026
Hydrochloric Acid → HCID 21475315, compound
https://huagongshe.com/reaction/982497
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,2,4-Trichloro-4-cyanobutanoyl chloride | HCID 11791149 | — |
| Product | HCID 21475315 | HCID 21475315 | — |
Reaction Steps
The cyclization reaction may be conveniently conducted in a batch reaction or in a continuous fashion in a coil reactor. In a typical reaction, 2,2,4-trichloro-4-cyanobutanoyl chloride is diluted with the desired solvent in a closed pressure vessel, and the vessel is pressurized with anhydrous HCl to the desired pressure. The reaction mixture is stirred at the appropriate temperature until the reaction is completed, usually from about one to about three hours. The reaction vessel is vented and the product, 3,3,5,6-tetrachloro-3,4-dihydropyridin-2-one, can be isolated by conventional procedures. For example, evaporation of the solvent provides a crude solid product which can be slurried with an aliphatic hydrocarbon, such as hexane, and which can then be isolated by filtration. Product so obtained is sufficiently pure after drying to be used in the subsequent aromatization. Alternatively, the crude reaction mixture can be used directly, immediately after venting and removal of the HCl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04996323 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-399dd2af1177448c9cc67ccbe24bc21a |
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| Source note | uspto-grants-1991_02 |
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