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HRID 1974371作成日:2026年10月26日

Methanol → 1-(3,4-Dimethylphenyl)-2,2-dimethylpropan-1-one

https://huagongshe.com/reaction/1974371

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Ammonium ChlorideHCID 25517—
反応物3,4-Dimethylbenzoyl chlorideHCID 2758535—
反応物HCID 178418306HCID 178418306—
触媒HCID 178505381HCID 178505381—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3,4-Dimethylphenyl)-2,2-dimethylpropan-1-oneHCID 15466857—

反応条件

温度-20 °C

反応手順

A suspension of 25.9 g. (0.15 mole) of phenyl thio copper in 1 liter dry tetrahydrofuran is cooled to -20° C. and treated by the dropwise addition of 120 ml. t-butyl lithium (0.149 mole, 1.24 M in pentane) for about 20 minutes maintaining the temperature at -20° C. The resulting green solution is stirred at -20° C. for 5 minutes and then cooled to -72° C. and treated by the dropwise addition of 17.8 g. (0.107 mole) 3,4-dimethyl-benzoyl chloride in 50 ml. tetrahydrofuran for about 20 minutes. The mixture is then stirred at -22° C. for 11/2 hours and then treated with 100 ml. methanol and allowed to warm to room temperature and then hydrolyzed by the addition of 250 ml. saturated ammonium chloride. The resulting solids are filtered and washed with tetrahydrofuran. The filtrate is dried over anhydrous magnesium sulfate, filtered and evaporated and the oil distilled to give 3',4' -dimethylpivalophenone; (b.p. 73°-76° C. at 0.1 mm).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04000307
出典データセットuspto-grants-1976_12
ORD IDord-02aae9f3867c46ec8784a1ed07272163
出典メモuspto-grants-1976_12