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HRID 1650773作成日:2026年10月27日
Tetrahydrofuran → 2,6-dichloro-4-trifluoromethoxyphenyl-5-(N,N-diethylamino)-3-(tert-butyl)-1H-1,2,4-triazole
https://huagongshe.com/reaction/1650773
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Diethylcyanamide | HCID 12050 | — |
| 反応物 | HCID 86743925 | HCID 86743925 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2,6-dichloro-4-trifluoromethoxyphenyl-5-(N,N-diethylamino)-3-(tert-butyl)-1H-1,2,4-triazole | HCID 14624364 | 87.1% |
反応手順
7.3 g (0.02 mol) of 2,2-dimethylpropionyl chloride 2,6-dichloro-4-trifluoromethoxyphenylhydrazone and 2.0 g (0.02 mol) of N,N-diethylcyanamide were added to 100 ml of tetrahydrofuran, and 2.2 g (0.02 mol) of triethylamine was dropwise added under reflux and stirring. After completion of the dropwise addition, the mixture was stirred at the same temperature for 0.5 hour. After cooling, the reaction solution was poured into water, and the precipitate was extracted with chloroform. The chloroform layer was washed with water and dried, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain 7.4 g (yield: 87.1%) of the desired compound as a pale yellow liquid. Refractive index nD20 : 1.4940.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04925864 |
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| 出典データセット | uspto-grants-1990_05 |
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| ORD ID | ord-eb05cccaa5ee4164ab241518e4b43c55 |
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| 出典メモ | uspto-grants-1990_05 |
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