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HRID 1105615作成日:2026年10月27日

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

https://huagongshe.com/reaction/1105615

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 19966334—
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 hours 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-methoxyvaleronitrile (4.0 g) as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04309442
出典データセットuspto-grants-1982_01
ORD IDord-791213980e6741aea291d0ca425a56ec
出典メモuspto-grants-1982_01