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Benzene → 4-(2,4-Dichlorobenzoyl)-1-methyl-5-(p-acetylbenzyloxy)pyrazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzene | HCID 241 | — |
| 反応物 | 1-[4-(Bromomethyl)phenyl]ethan-1-one | HCID 583785 | — |
| 反応物 | HCID 178481842 | HCID 178481842 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | 4-(2,4-Dichlorobenzoyl)-1-methyl-5-(p-acetylbenzyloxy)pyrazole | HCID 15590728 | 83% |
反応手順
In 30 ml of dry benzene containing 0.50 g (0.005 mol) of triethylamine was dissolved 1.36 (0.005 mol) of 4-(2,4-dichlorobenzoyl)-1-methyl-5-hydroxypyrazole, and then 1.07 g (0.005 mol) of p-acetylbenzylbromide was added thereto. The resulting mixture was heated under reflux for 3 hours. After cooling the reaction mixture, the salt precipitated was filtered off and the solvent was distilled off therefrom under reduced pressure. The resulting oil was purified through column chromatography on silica gel using benzene/ethyl acetate 8:1 as an eluent to give 1.67 g of the title compound (yield 83%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04557753 |
| 出典データセット | uspto-grants-1985_12 |
| ORD ID | ord-70c3c8650efc4dc0acd3abc0a8cb70b0 |
| 出典メモ | uspto-grants-1985_12 |