HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2,4,6-Trihydroxymethyl-s-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2,4,6-Triethyl 1,3,5-triazine-2,4,6-tricarboxylate | HCID 13478 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,4,6-Trihydroxymethyl-s-triazine | HCID 22323664 | — |
Reaction Steps
2,4,6-Triethoxycarbonyl-s-triazine (1 g, 3.36 mmol) is dissolved in dichloromethane (15 mL) and absolute ethanol (25 mL) then cooled to 0° C. before sodium borohydride (127 mg, 3.36 mmol) is added. After 15 minutes calcium chloride (373 mg, 2.97 mmol) is added and the reaction mixture is warmed to room temperature. The reaction mixture is dried to a yellow solid and subjected to soxhlet extraction with ethanol. The ethanol is evaporated to a white solid. The product is crystallized from Methanol and water or purified by silica gel flash column chromatography to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06942966B1 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-d5bdd8ccfeb541478b6a09817d4aa8b7 |
| Source note | uspto-grants-2005_09 |