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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | N-Dodecylacrylamide | HCID 73929 | — |
| Reactant | 2,2'-Azobis(2-methylpropanimidamide) dihydrochloride | HCID 76344 | — |
| Reactant | N,N-Dimethylaminopropyl acrylamide | HCID 77452 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | N-[3-(dimethylamino)propyl]acrylamide acrylamide N-dodecylacrylamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06299868B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-2b62860f913e4f248f0e0a0dc4c5d1e1 |
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| Source note | uspto-grants-2001_10 |
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