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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612425Generated: October 30, 2026

Triethylamine → N-(2,4-dichlorophenyl)ethanehydrazonoyl chloride

https://huagongshe.com/reaction/1612425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(2,4-Dichlorophenyl)hydrazineHCID 408929—
ReactantEthanimidic acid, ethyl ester, hydrochloride (1:1)HCID 2724290—
CatalystEthanimidic acid, ethyl ester, hydrochloride (1:1)HCID 2724290—
SolventDichloromethaneHCID 6344—
ProductN-(2,4-dichlorophenyl)ethanehydrazonoyl chlorideHCID 7281503193.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution of 13.6 grams (0.1100 mole) of ethyl acetimidate hydrochloride and 13.2 grams (0.1300 mole) of triethylamine in 100 grams of methylene chloride was cooled to about 0° C. for five minutes, and 17.7 grams (0.1000 mole) of 2,4-dichlorophenylhydrazine (1) was added. Upon completion of addition the reaction mixture stirred at 0° C. for about one hour, then it was allowed to warm to ambient temperature where it stirred for about two hours. GC analysis of the reaction mixture indicated the presence of a small amount of unreacted (1). An additional 0.6 gram of ethyl acetimidate hydrochloride was added (total 14.2 gram—0.1150 mole), and the reaction mixture was stirred for an additional one hour. After this time the reaction mixture was washed with about 20 mL of water and dried with magnesium sulfate. The mixture was filtered, and the filtrate was concentrated under reduced pressure to a semi-solid residue. The residue was triturated with 20 mL of hexane, and the resultant solid was collected by filtration. The solid was washed with 50 mL of hexane and dried, yielding 20.4 grams (93.4% yield) of 2-(2,4-dichlorophenyl)hydrazidethaneimidic acid (A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06992221B2
Source datasetuspto-grants-2006_01
ORD IDord-201adbbde2794dbcbe2f6b4114297da0
Source noteuspto-grants-2006_01