HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112361Generated: October 25, 2026
Acrylonitrile → 1-Propanamine, 3-(octadecyloxy)-
https://huagongshe.com/reaction/2112361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Stearyl Alcohol | HCID 8221 | — |
| Catalyst | Nickel | HCID 935 | — |
| Catalyst | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Propanamine, 3-(octadecyloxy)- | HCID 82087 | 89.8% |
Reaction Steps
An autoclave equipped with a stirrer and a temperature gage was charged with 270.5 g of octadecanol and 0.1 g of potassium hydroxide and the mixture was dehydrated at 120° C. under a vacuum of 2.6 kPa for one hour. Then, the mixture was cooled to 60° C. and 58.4 g of acrylonitrile was introduced into the autoclave over one hour, which was then kept as it was for one hour to complete the reaction. Next, 1.9 g of Raney nickel, 0.3 g of sodium hydroxide and 16.1 g of ion exchange water were introduced into the autoclave, which was then reacted for hydrogenation and reduction at 130° C. for 3 hours. Then, the reaction mixture was subjected to filtration to remove the catalyst, distilled and refined to obtain 294.3 g of a corresponding 3-octadecyloxypropylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524486B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-6c971d9795d346a284c2b0c0040726c8 |
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| Source note | uspto-grants-2009_04 |
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