HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762067Generated: October 31, 2026
Potassium Hydroxide → HCID 70394092, compound
https://huagongshe.com/reaction/1762067
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine | HCID 104556 | — |
| Reactant | Oleic Acid | HCID 445639 | — |
| Reactant | Methyl Oleate | HCID 5364509 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70394092 | HCID 70394092 | — |
Reaction Steps
A mixture of 20 g of 1,3,5-tris-hydroxyethyl perhydro-s-triazine from the method of Paquin, Ber., 82, 316 (1949) and 0.30 g (5.8 mole percent) of powdered KOH is heated at 80° C. under reduced pressure (less than 0.1 mm) for 6 hours. Methyl oleate (30g ) from acid-catalyzed esterification of oleic acid in methanol is then added and the resulting mixture (in two phases) is stirred at 80° C. under the reduced pressure overnight. The homogeneous material which is obtained is dissolved in CH2Cl2, washed with water, dried over potassium carbonate, then is concentrated into a light yellow oil of 41 g (84.9 percent of theory). Both the infrared (1745 cm-1) and nuclear magnetic resonance spectra are consistent with the desired 1,3,5-triazine-1,3,5-(2H,4H,6H)triethanol monooleate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04830827 |
|---|
| Source dataset | uspto-grants-1989_05 |
|---|
| ORD ID | ord-8f906b779172474e8c267f095306dbe3 |
|---|
| Source note | uspto-grants-1989_05 |
|---|