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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442028Generated: October 30, 2026

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

https://huagongshe.com/reaction/442028

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 2N hydrochloric acid. The acid extract was then made basic with 30ml of 2N 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 numberUS04044023
Source datasetuspto-grants-1977_08
ORD IDord-d7024198808444cca8cf9a8917e129a7
Source noteuspto-grants-1977_08