関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | 4-Chloro-2-methylphenol | HCID 14855 | — |
| 反応物 | Benzene, 1-(chloromethyl)-4-(1,1-dimethylethyl)- | HCID 88198 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 2-[(4-tert-Butylphenyl)methyl]-4-chloro-6-methylphenol | HCID 71414064 | — |
反応手順
106.5 g (0.75 mol) 4-chloro-2-methylphenol and 45.67 g (0.25 mol) 4-tert. butylbenzylchloride are dissolved in 200 ml chloroform, and 22.5 g water-free zinc chloride are added as Friedel-Crafts catalyst. Thereafter the reaction mixture is stirred, whereby indeed at room temperature to the start of the reaction intense gas development, i.e. intense reaction, is to be noted. Subsequently the reaction mixture is stirred at 60° C. 5-6 h and washed three times each with 200 ml water for the purpose of removing the zinc chloride. The organic phase is dried across magnesium sulfate and the chloroform is driven off in a vacuum. At 182°-185° C./0.3 Torr the 4-chloro-2-methyl-6-(4'-tert. butylbenzyl)-phenol distills over as water-clear, viscous, nearly odorless liquid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04532367 |
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| 出典データセット | uspto-grants-1985_07 |
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| ORD ID | ord-10fcae91893c403881b74948e7c2dc88 |
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| 出典メモ | uspto-grants-1985_07 |
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