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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834902Generated: October 31, 2026

(Aminooxy)acetic acid → HCID 3372981, compound

https://huagongshe.com/reaction/1834902

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Aminooxy)acetic acidHCID 286—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium AcetateHCID 517045—
SolventEthanolHCID 702—
ProductHCID 3372981HCID 3372981—

Reaction Steps

4.2 g of 4-chlorobenzaldehyde and 3.3 g of hemihydrochloride of amino-oxyacetic acid were dissolved in 50 ml of 90% ethanol. The solution was mixed with 7.4 g of sodium acetate and then refluxed for 20 minutes. The reaction mixture was subsequently concentrated by evaporation in a vacuum. After an excess of 2N sodium hydroxide had been added, the residue was twice extracted with ether, after which the remaining aqueous solution was acidified with 2N hydrochloric acid and again extracted twice with ether. The latter ethereal solution was washed twice with water, then dried over anhydrous sodium sulfate and subsequently concentrated by evaporation. The residue was crystallized from a mixture of ether and petroleum ether, then from highly dilute ethanol and ultimately twice from a mixture of benzene and petroleum ether. The substance obtained melted at 121°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04071686
Source datasetuspto-grants-1978_01
ORD IDord-2aa241e035b14e8499775b4e3ae35bfe
Source noteuspto-grants-1978_01