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HRID 561462作成日:2026年10月27日

Water → 4-Chloro-alpha-cyclopropyl-alpha-methylbenzenemethanol

https://huagongshe.com/reaction/561462

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物AcetonitrileHCID 6342—
反応物P-ChloroacetophenoneHCID 7467—
反応物HCID 178418630HCID 178418630—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物4-Chloro-alpha-cyclopropyl-alpha-methylbenzenemethanolHCID 23463—

反応条件

温度0 °C

反応手順

1.50 g (9.70 mmol) of 4-chloroacetophenone were dissolved in 8 ml of diethyl ether at 0° C., and 38.8 ml (19.41 mmol) of a 0.5N solution of cyclopropylmagnesium bromide in tetrahydrofuran were slowly added dropwise. Stirring at 0° C. for 1 h was followed by warming to RT, addition of water and acetonitrile to the reaction solution, and filtration of the mixture through kieselguhr. The organic solvents were removed in a rotary evaporator, and the aqueous phase was extracted twice with diethyl ether. The combined organic phases were washed with saturated aqueous sodium chloride solution, and the solvents were removed in vacuo. The crude product was purified twice by preparative HPLC (mobile phase: acetonitrile/water gradient). The acetonitrile was removed from the combined product phases in a rotary evaporator, and the aqueous phase was extracted twice with diethyl ether. The combined organic phases were again washed with saturated aqueous sodium chloride solution, dried over sodium sulfate and filtered, and the solvents were removed in vacuo. 1.37 g (72% of theory) of the title compound were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063234B2
出典データセットuspto-grants-2011_11
ORD IDord-c7474b85547b455f9308765e46716d1f
出典メモuspto-grants-2011_11