HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841109Generated: October 27, 2026
Hydrochloric Acid → N-Octadecanoylacrylamide
https://huagongshe.com/reaction/841109
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | Stearoyl chloride | HCID 8212 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-Octadecanoylacrylamide | HCID 22620855 | — |
Reaction Steps
Into a 250 -mL-capacity conical flask equipped with an anhydrous calcium chloride (CaCl2) guard tube, 15.1 g 1-octadecanoyl chloride [CH3—(CH2)16—COCl] (0.005 M). 3.5 g acrylamide (CH2═CH—CO—NH2) (0.05 M), and 50 ml acetone were placed to obtained a clear solution. The solution was stirred with a magnetic needle at room temperature. Anhydrous zinc chloride (ZnCl2), 6.5 g (0.05 M), was added and the reaction mixture was stirred at room temperature. After 5-10 min of stirring, vigorous evolution of hydrogen chloride took place which ceased after about 5 min. The temperature of reaction mixture was increased to 40-50° C. It was then cooled to room temperature and poured into 500 ml cold distilled water. A white product precipitated. The product was isolated and purified by reprecipitation from acetone into cold water. The purified product was dried in a vacuum desiccator.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06369249B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-61f5b8dc43de47549b7bf44a6c4547d3 |
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| Source note | uspto-grants-2002_04 |
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