HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Oxide → 2-(Hexylamino)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Hexylamine | HCID 8102 | — |
| Reactant | 1-Aminooctan-2-ol | HCID 345053 | — |
| Product | 2-(Hexylamino)ethanol | HCID 108610 | — |
Reaction Steps
In an alternate synthesis scheme for n-hexyl ethanolamine, the ethoxylation steps remained the same as above in sequence, temperature and pressure. However, the preferred weight fraction of n-hexyl amine to ethylene oxide was lowered to approximately 88 pounds n-hexyl amine to 12 pounds ethylene oxide to yield 100 pounds of reaction mass. The weight ratio of mono to di ethoxylates in the reaction mass was approximately 4.0-4.2 mono to 1.0 di. The purification section was also the same except the process was stopped after removal of n-hexyl amine overhead. The final bottoms fraction contained n-hexyl ethanolamine and some diethoxylates byproducts (less than 20% by weight).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04749503 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-e5f634985f7b4e9f98e9fa40ea5a8cef |
| Source note | uspto-grants-1988_06 |