HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359516Generated: October 25, 2026
Phosphorus oxychloride → N-(2,4-dichlorophenyl)ethanehydrazonoyl chloride
https://huagongshe.com/reaction/1359516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Acetic acid N'-(2,4-dichloro-phenyl)-hydrazide | HCID 612615 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(2,4-dichlorophenyl)ethanehydrazonoyl chloride | HCID 72815031 | 78.5% |
Reaction Steps
A solution of 25.0 grams (0.1142 mole) of 1-acetyl-2-(2,4-dichlorophenyl)-hydrazine (2) in 120 grams of toluene was stirred, and 17.7 grams (0.1142 mole) of phosphorus oxychloride was added portionwise. Upon completion of addition the reaction mixture was warmed to about 110° C. where it stirred for about 30 minutes. GC analysis of the reaction mixture after this time indicated the reaction was complete. An additional 100 grams of toluene was added to the reaction mixture, and the solution was decanted into a separatory funnel. A residue in the reaction vessel was washed with about 40 grams of toluene, and the wash was also decanted into the separatory funnel. The toluene solution was then washed with an aqueous solution of 10% potassium carbonate. The aqueous layer was back-washed with two 75 gram portions of toluene. The combined toluene layer and washes was dried with magnesium sulfate. The mixture was filtered and the filtrate was concentrated under reduced pressure, yielding 21.3 grams (78.5% yield) of N-(2,4-dichlorophenyl)-ethanehydrazonoyl chloride (A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06600049B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-aea4e46243bb45bd8f95c0585d716a95 |
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| Source note | uspto-grants-2003_07 |
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