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HRID 371522作成日:2026年10月26日

Water → 2-[(4-tert-Butylphenyl)methyl]-4-chloro-6-methylphenol

https://huagongshe.com/reaction/371522

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-Chloro-2-methylphenolHCID 14855—
反応物Benzene, 1-(chloromethyl)-4-(1,1-dimethylethyl)-HCID 88198—
溶媒ChloroformHCID 6212—
生成物2-[(4-tert-Butylphenyl)methyl]-4-chloro-6-methylphenolHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04532367
出典データセットuspto-grants-1985_07
ORD IDord-10fcae91893c403881b74948e7c2dc88
出典メモuspto-grants-1985_07