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1,4-Dioxane → 2-(4-Acetoxybenzoylamino)-4-octylphenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,4-Dioxane | HCID 31275 | — |
| 反応物 | Phenol, 2-amino-4-octyl- | HCID 87767 | — |
| 反応物 | p-Acetoxybenzoyl chloride | HCID 2756254 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 2-(4-Acetoxybenzoylamino)-4-octylphenol | HCID 19021155 | 70.8% |
反応手順
In a 100 ml round-bottom flask, the resultant 4-acetoxybenzoic chloride, 3.10 g (15.1 m mole) of 2-amino-4-octylphenol and 40 ml of dioxane were placed and heated to keep inner temperature 85 to 88.5° C. To the mixture, 5.5 ml of pyridine was added dropwise under stirring, followed by heating and stirring for 20 minutes at 85 to 88.5° C. After the reaction, the reaction mixture was cooled with ice and poured into ca. 200 ml of ice water to precipitate a crystal. The crystal was filtered, washed and recrystallized from methanol to obtain 4.10 g of 2-(4-acetoxybenzoylamino)-4-octylphenol (Yield: 70.8%). ##STR79##
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05244596 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-9cf256dca8e143efbbadb3597f087187 |
| 出典メモ | uspto-grants-1993_09 |