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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantAcetic acid N'-(2,4-dichloro-phenyl)-hydrazideHCID 612615—
SolventTolueneHCID 1140—
ProductN-(2,4-dichlorophenyl)ethanehydrazonoyl chlorideHCID 7281503178.5%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06600049B2
Source datasetuspto-grants-2003_07
ORD IDord-aea4e46243bb45bd8f95c0585d716a95
Source noteuspto-grants-2003_07