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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606748Generated: October 25, 2026

Hydrochloric Acid → Acrylamide

https://huagongshe.com/reaction/1606748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantUreaHCID 1176—
ReactantAcrylamideHCID 6579—
ReactantAcrylonitrileHCID 7855—
ReactantAmmonium PersulfateHCID 62648—
ReactantSodium PyrosulfiteHCID 656671—
ReactantSodium vinylsulfonateHCID 3270262—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventOxygenHCID 977—
ProductAcrylamideHCID 6579—
ProductAcrylonitrileHCID 7855—
ProductVinylsulfonic acidHCID 62474—

Reaction Steps

A water-soluble copolymer of acrylonitrile, acrylamide and ethylene sulfonic acid was prepared in the following way: 57.5 g of an aqueous 47% solution of sodium ethylene sulfonate, stabilized against polymerization by 0.2% sodium nitrite, was destabilized by adding 3 g urea and acidified with concentrated hydrochloric acid to pH 2. The developing gases were repeatedly drawn off. 7.1 g Acrylamide and 13.6 ml acrylonitrile were added and the monomer mixture was dissolved in 76 ml of oxygen-free water. 1 ml of a 5% sodium pyrosulfite solution and the same amount of ammonium persulfate were stirred in, and the somewhat turbid solution was left standing under carbon dioxide at room temperature for 24 hours. The viscous solution thus obtained was poured into 2 liters of anhydrous ethanol. The white coagulate was purified by dissolving it in water and again precipitating it in anhydrous ethanol, broken to small pieces and dried at 70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953545
Source datasetuspto-grants-1976_04
ORD IDord-035102b7b2114125aea921d27431fc01
Source noteuspto-grants-1976_04