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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379502Generated: October 25, 2026

Hydrochloric Acid → N-[3-(dimethylamino)propyl]acrylamide acrylamide N-dodecylacrylamide

https://huagongshe.com/reaction/379502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcrylamideHCID 6579—
ReactantN-DodecylacrylamideHCID 73929—
Reactant2,2'-Azobis(2-methylpropanimidamide) dihydrochlorideHCID 76344—
ReactantN,N-Dimethylaminopropyl acrylamideHCID 77452—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductN-[3-(dimethylamino)propyl]acrylamide acrylamide N-dodecylacrylamideHCID 86757470—

Reaction Steps

A solution of N-[3-(dimethylamino)propyl]acrylamide (22.5 g), acrylamide (2.7 g), and N-dodecylacrylamide (2.3 g) in deionized water (30 mL) and ethanol (30 mL) was heated to 60° C. under a nitrogen atmosphere. When the solution reached 60° C., 2,2′-azobis(2-amidinopropane)dihydrochloride (1.4 g of a 20 percent aqueous solution) was added. Heating was continued for 18 hours under a nitrogen atmosphere. After cooling to room temperature, the reaction solution was dissolved in isopropanol (150 mL), and concentrated HCl (29.2 g) was added with stirring. The solution was decanted from the precipitated polymer. The polymer was suspended in isopropanol (500 mL), stirred for at least 15 minutes, and allowed to settle. After decanting, the polymer was similarly washed an additional 3 times with isopropanol. The washed polymer was dried in a forced-air oven at 70° C. to afford 34.7 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06299868B1
Source datasetuspto-grants-2001_10
ORD IDord-2b62860f913e4f248f0e0a0dc4c5d1e1
Source noteuspto-grants-2001_10