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HRID 51008作成日:2026年10月26日

Tetrahydrofuran → 1-Cyclopropyl-1-(4-fluorophenyl)ethanol

https://huagongshe.com/reaction/51008

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Cyclopropyl-4-fluorophenyl ketoneHCID 53737258—
反応物HCID 178418573HCID 178418573—
溶媒Diethyl EtherHCID 3283—
生成物1-Cyclopropyl-1-(4-fluorophenyl)ethanolHCID 9810489%

反応手順

To a solution of cyclopropyl-4-fluorophenyl ketone (523 mg, 3.19 mmol) in THF (10 mL) at 0° C. under N2 was added 3 M methyl magnesium bromide (1.7 mL, 5.1 mmol) in Et2O. After 90 minutes at 0° C., the reaction was quenched by addition of brine (10 mL) and diluted with Et2O (100 mL). The organic solution was washed with saturated NaHCO3 (100 mL) and brine (100 mL). Column purification (hexanes:EtOAc 9:1) yielded 1-cyclopropyl-1-(4-fluorophenyl)ethanol (512 mg, 89%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713471B1
出典データセットuspto-grants-2004_03
ORD IDord-83ca91197072490fa4518362b94b5cc9
出典メモuspto-grants-2004_03