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HRID 1252563作成日:2026年10月25日

Sodium Cyanide → 2-Amino-2-(fluoromethyl)-5-methoxypentanenitrile

https://huagongshe.com/reaction/1252563

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CyanideHCID 8929—
反応物Acetonitrile, fluoro-HCID 10420—
反応物Ammonium ChlorideHCID 25517—
反応物1-Chloro-3-methoxypropaneHCID 118927—
反応物MagnesiumHCID 5462224—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2-Amino-2-(fluoromethyl)-5-methoxypentanenitrileHCID 1996633499.9%
生成物HCID 178495109HCID 178495109—

反応条件

温度-30 °C

反応手順

Under an atmosphere of nitrogen, 3-methoxypropyl magnesium chloride is prepared from 3-methoxy-1-chloropropane (5.43 g, 50 mmol), prepared according to Haworth and Perkin, Chem. Zentralblatt, II, 1271 (1912) and magnesium turnings (1.22 g, 50 mmol) in dry THF (50 ml). The mixture is heated under reflux for 3 hours, then cooled to -30° C. and a solution of fluoroacetonitrile (2.95 g, 50 mmol) in THF (30 ml) is added during 20 minutes. After keeping the mixture at -30° C. for 1/2 hour more, a solution of sodium cyanide (4.9 g, 100 mmol) and ammonium chloride (8.09 g, 150 mmol) in water (100 ml), previously cooled to 0° C., is added and the mixture is stirred for 3/4 hour at room temperature. After saturating with sodium chloride, the THF layer is separated and the aqueous phase is extracted twice with ether. After drying (Na2SO4), the combined organic extracts are evaporated to give 2-fluoromethyl-2-amino-5-methoxypentanenitrile (4.0 g) as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04743691
出典データセットuspto-grants-1988_05
ORD IDord-2b7703a477ff49669e7de67f7572a85c
出典メモuspto-grants-1988_05