関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hexamethylenetetramine | HCID 4101 | — |
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | 2-tert-Butyl-6-methylphenol | HCID 16678 | — |
| 生成物 | 3-tert-Butyl-4-hydroxy-5-methylbenzaldehyde | HCID 12467986 | — |
反応手順
Under a nitrogen atmosphere, 76.65 g of 2-(1,1-dimethylethyl)-6-methylphenol (Aldrich), 65.42 g of hexamethylenetetramine and 700 ml of trifluoroacetic acid were stirred at reflux temperature for about 24 hours, then allowed to cool and evaporated. The residue from the evaporation was taken up in 1500 ml of water and 1000 ml of chloroform and neutralized to pH 7 with solid sodium carbonate. The resultant layers were separated and the aqueous layer was washed with chloroform. The organic layer was dried over sodium sulfate overnight, after which it was again washed with a volume of chloroform and evaporated. The resultant residue was then taken up in 375 ml of toluene, heated on a steam bath and then allowed to cool to room temperature overnight. Subsequent workup gave 28.3 g of the desired subtitled intermediate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05731336 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-e337e55a1fd94b369c26bae4adbf39ba |
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| 出典メモ | uspto-grants-1998_03 |
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