関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-tert-Butylphenol | HCID 7393 | — |
| 反応物 | 1-Butanol, 4-chloro-, 1-acetate | HCID 23399 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Phenolate | HCID 119047 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-(4-Tert-butylphenoxy)butyl acetate | HCID 13313736 | — |
反応手順
To a stirred slurry of 1.6 g sodium hydride (as 50% dispersion in oil) in 50 ml dry dimethyl formamide was added, drop-wise, a solution of 5.0 g p-tert-butylphenol (33.3 mmoles) in 50 ml dry dimethyl formamide and the solution stirred under nitrogen until the phenoxide had totally formed. To the phenoxide was added a solution of 5.0 g 4-chlorobutyl acetate (33.3 mmoles) in 50 ml dry dimethyl formamide and the solution was stirred for fourteen hours. The reaction mixture was partitioned between water/toluene. The organic layer was removed, washed with water, then 1N sodium bicarbonate. The organic layer was removed, dried and evaporated to an orange oil, 5.6 g. The oil was chromatographed on 500 g, 90 to 200 mesh silica gel (CH2Cl2 eluent) yielding pure 4-(p-tert-butylphenoxy)-butyl acetate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05242936 |
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| 出典データセット | uspto-grants-1993_09 |
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| ORD ID | ord-cebef95bc8384043b4a84d71a6aab475 |
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| 出典メモ | uspto-grants-1993_09 |
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