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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733473Generated: November 2, 2026

2-Chloro-N,N-dimethylethylamine → HCID 85439121, compound

https://huagongshe.com/reaction/1733473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-N,N-dimethylethylamineHCID 7901—
Reactant2-[1-(4-chlorophenyl)ethylideneamino]oxyacetic AcidHCID 2821257—
ReactantSodiumHCID 5360545—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 85439121HCID 85439121—

Reaction Steps

4.3 g of 2-chloro-N,N-dimethyl ethylamine was added to a suspension of 10 g of the sodium salt of (4-chloro-α-methylbenzylidene)amino-oxyacetic acid in 30 ml of dimethylformamide. The mixture was stirred for 72 hours. It was then diluted with water and extracted with diethylether. The resulting ethereal solution was extracted with 20 ml of 2 N hydrochloric acid. The acid extract was then made basic with 30 ml of 2 N sodium hydroxide and extracted with diethylether. The latter ethereal extract was washed, dried over anhydrous sodium sulphate and after concentration by evaporation neutralized with alcoholic hydrochloric acid. When diethylether was added the hydrochloride of the (2-dimethyl-aminoethyl)ester of (4-chloro-α-methylbenzylidene) aminooxyacetic acid crystallized out. It was recrystallized from an alcohol-ether mixture; melting point 160°-162° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242348
Source datasetuspto-grants-1980_12
ORD IDord-29b3e47b7ca242c49bab54751d658489
Source noteuspto-grants-1980_12