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HRID 1065677생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1065677

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CyanideHCID 8929—
반응물Acetonitrile, fluoro-HCID 10420—
반응물Ammonium ChlorideHCID 25517—
반응물1-Chloro-3-methoxypropaneHCID 118927—
반응물MagnesiumHCID 5462224—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-Amino-2-(fluoromethyl)-5-methoxypentanenitrileHCID 19966334—
생성물HCID 178495109HCID 178495109—

반응 조건

온도-30 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04330559
출처 데이터셋uspto-grants-1982_05
ORD IDord-63f2d3c1f3a04870a6a268b8fcf77aca
출처 메모uspto-grants-1982_05