HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1,3,5-Triazin-2-amine, 4-ethoxy-6-(trifluoromethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | HCID 178418324 | HCID 178418324 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,3,5-Triazin-2-amine, 4-ethoxy-6-(trifluoromethyl)- | HCID 199947 | 89% |
Reaction Steps
8.4 g (0.1 mol) of cyanoguanidine and 35.5 g (0.25 mol) of ethyl trifluoroacetate are initially introduced into 46 g of ethanol, and a suspension of 8.5 g (0.125 mol) of sodium ethoxide in 39.8 g of ethanol is added in the course of 5 min. After the addition of 5.66 g (0.05 mol) of calcium chloride, the reaction mixture is heated to reflux for 7 hours. 0.5 ml of a conc. hydrochloric acid is then added at 20° C. and the ethanol is removed. 100 g of water are added and the suspension is filtered with suction. The residue is washed with 50 ml of water and dried at 50° C./20 mbar. 18.6 g (0.089 mol, 89%) of 2-amino-4-ethoxy-6-trifluoromethyl-1,3,5-triazine are obtained in the form of a colorless powder (HPLC: 99.8 area %, m.p. 124°-125° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05739328 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-332a7fc1d056469db36fcd54e4fb80fa |
| Source note | uspto-grants-1998_04 |