HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 86741141, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acrylate | HCID 25188 | — |
| Reactant | Oleylamine | HCID 5356789 | — |
| Product | HCID 86741141 | HCID 86741141 | — |
Reaction Steps
When an amide of a fatty amine is desired, i.e. a compound wherein X is --CH2 --NR4R5, it is convenient to acylate and, optionally, alkylate a compound such as oleyl amine and then hydroformylate and acrylate as described above. For example, oleyl amine can be acetylated with acetic acid and methylated to form N-acetyl-N-methyl oleyl amine. This unsaturated amine can then be reacted with carbon monoxide and hydrogen to prepare N-acetyl-N-methyl-10(11)-formyl octadecanamine. This formylated amine can then be reduced to prepare N-acetyl-N-methyl-10(11)-hydroxymethyloctadecanamine which is finally reacted with an acryloyl compound to prepare N-acetyl-N-methyl-10(11)-acryloxymethyloctadecacamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04626582 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-7d53887c9f344daca91e49c6fbd54d6b |
| Source note | uspto-grants-1986_12 |