HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azelaic Acid → Bis(2-hydroxyethyl) azelate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azelaic Acid | HCID 2266 | — |
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | Bis(2-hydroxyethyl) azelate | HCID 122426 | — |
Reaction Steps
The reaction of 0.25 moles azelaic acid with 0.55 moles ethylene oxide under pressure using methyl isobutyl ketone in the presence of the catalyst of Example II (0.15% by wt. of total system) at 153° C gave bis(2-hydroxyethyl)azelate in quantitative crude yield. The material was isolated as a grey-white solid melting at 46°-47° C from a n-butyl chloride-acetone mixture in 88.5% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04017429 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-d48dd62d737a4192a0aaa9197f7a2d56 |
| Source note | uspto-grants-1977_04 |