HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(5-t-Butyloxadiazol-3-yl)-3-chloro-2'-methyl-4'-trifluoromethoxybenzanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methyl-4-(trifluoromethoxy)aniline | HCID 2775546 | — |
| Reactant | 2-(5-t-Butyloxadiazol-3-yl)-3-chlorobenzoyl chloride | HCID 18003335 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(5-t-Butyloxadiazol-3-yl)-3-chloro-2'-methyl-4'-trifluoromethoxybenzanilide | HCID 18003338 | 29% |
Reaction Steps
0.5 Gram of 2-(5-t-butyloxadiazol-3-yl)-3-chlorobenzoyl chloride was dissolved in 30 ml of tetrahydrofuran, and 0.3 g of 2-methyl-4-trifluoromethoxyaniline and 0.2 g of triethylamine were added thereto, the reaction was carried out for 1 hour under stirring. After completion of the reaction, the reaction mixture was poured into water, after extraction of the objective product with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, the solvent was removed by distillation under reduced pressure, the residue thus obtained was purified by a silica gel column chromatography to obtain 0.22 g (yield: 29%) of the objective product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06642379B1 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-46b911b38fe9446d812cefdcf33b7e27 |
| Source note | uspto-grants-2003_11 |