HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Oxide → HCID 54110719, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | HCID 53786409 | HCID 53786409 | — |
| Catalyst | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Product | HCID 54110719 | HCID 54110719 | 62.4% |
Reaction Steps
26.4 g of ethylene oxide are introduced into 82.5 g of 4-(5-methyl-1-phenyl-3-hexyl)-1,2,4-triazolidine-3,5-dione (starting material 9) and 0.3 g of trimethyl benzyl ammonium hydroxide in 150 g of dimethyl acetamide. The solvent is distilled off in vacuo, the residue is dissolved by heating in 150 ml of ethyl acetate, 10 g of powdered active carbon are added and the whole is filtered hot. A deposit crystallises out on cooling and is isolated by filtration under suction and dried, giving 68 g of 1,2-bis-(2-hydroxyethyl)-4-(5-methyl-1-phenyl-3-hexyl)-1,2,4-triazolidine-3,5-dione in the form of colourless crystals melting at 114° C. IR- and NMR-spectra together with elemental analysis confirm the assumed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04377694 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-f6b7cced724a47b08092dfd7b9d11f05 |
| Source note | uspto-grants-1983_03 |