HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20437722, compound → 2,4-Diethoxy-6-(1-piperazinyl)-1,3,5-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20437722 | HCID 20437722 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 2,4-Diethoxy-6-(1-piperazinyl)-1,3,5-triazine | HCID 20437715 | 102.5% |
Reaction Steps
The product from (b) (3.25 g) in potassium hydroxide solution (1N, 20 ml) and ethanol (30 ml) was left at room temperature for 3 hours. Then further potassium hydroxide solution (20 ml) was added. After 45 minutes the reaction mixture was extracted with chloroform (5×30 ml), and the combined chloroform extracts dried (Na2SO4) and evaporated in vacuo to give 4,6-diethoxy-2-piperazino-1,3,5-triazine (3.0 g) as an oil. The product was characterized spectroscopically and used directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04483857 |
| Source dataset | uspto-grants-1984_11 |
| ORD ID | ord-950ab7042c1143b7ba9232604171f332 |
| Source note | uspto-grants-1984_11 |