HuagongsheHuagongshe Chemistry Print Report · For research reference only
Octadecylamine → HCID 13361750, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Octadecylamine | HCID 15793 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Product | HCID 13361750 | HCID 13361750 | — |
Reaction Steps
In the first process stage, glucose (a) is reacted with octadecylamine (b) to give N-octadecyl-β-D-glucopyranosylamine (c), which is acylated in the second process stage with oleyl chloride to give N-octadecyl-N-oleyl-β-D-glucopyranosylamine (d). In the third process stage, O-acylation is then carried out in position 6 by means of dodecanoyl chloride, and N-octadecyl-N-oleyl-(6-lauroyl-β-D-glucopyranosyl)-amide (I) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04574122 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-00a5c8ba21b745d39d6db184ed9de449 |
| Source note | uspto-grants-1986_03 |