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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974693Generated: October 30, 2026

Hydrochloric Acid → HCID 178442844, compound

https://huagongshe.com/reaction/974693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 19986110HCID 19986110—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178442844HCID 178442844—

Reaction Steps

11.12 g of hydroxylamine hydrochloride were added to a solution of 12.60 g of sodium hydroxide in a mixture of 80 ml of water and 100 ml of ethanol, whilst ice-cooling. A solution of the whole of the crude ethyl 3,3-ethylenedioxystearate prepared as described above in 200 ml of ethanol was added all at once, whilst ice-cooling, to the resulting mixture. The reaction mixture was then stirred at room temperature for 2 hours. At the end of this time, 100 ml of concentrated hydrochloric acid were added, and the mixture was heated under reflux for 1.5 hours. The mixture was allowed to cool, and the precipitated solid was collected by filtration and dissolved in methylene chloride. The methylene chloride solution was washed with a saturated aqueous solution of sodium bicarbonate and with water, dried and concentrated by evaporation under reduced pressure. The residue was filtered with the aid of suction to give 7.19 g of the title compound as crystals. An oily material (19 g) separated from the filtration was subjected to column chromatography through 250 g of alumina (grade III). From the fractions eluted with a 20:1 by volume mixture of methanol and acetic acid, an additional 0.82 g of crystals was obtained. These crystals melted at 81.5°-82.5° C. (from cold methylene chloride).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05068340
Source datasetuspto-grants-1991_11
ORD IDord-3213c249e7e54c97b7a076781ba8606f
Source noteuspto-grants-1991_11