HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 21463650, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Chloromethyl)-2-fluoro-4-(trifluoromethyl)benzene | HCID 21463583 | — |
| Reactant | HCID 136048655 | HCID 136048655 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21463650 | HCID 21463650 | 49.6% |
Reaction Steps
To 20 ml of N,N-dimethylformamide are added 3-(2-chloro-6-fluorophenyl) 5-[3-chloro-4-hydroxyphenyl)-1-methyl-1H-1,2,4-triazole (0.90 g) and potassium carbonate (0.40 g) and 2-fluoro-4-trifluoromethylbenzyl chloride (0.50 g) is added thereto at room temperature with stirring, which is stirred at 120° C. for 5 hours. On completion of the reaction, the reaction solution is cooled to room temperature, poured into water and extracted with ethyl acetate. The organic layer is washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate is purified by silica gel column chromatography to give 0.60 g of desired compound (melting point: 109.0°-111.0° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616594 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-71fe3788171140db82b4800747fbfa2c |
| Source note | uspto-grants-1997_04 |