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HRID 1607753생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1607753

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 1996633499.9%
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 Perking, 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 mol) 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 (Na2SO 4), the combined organic extracts are evaporated to give 2-fluoromethyl-2-amino-5-methoxypentanenitrile (4.0 g) as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04866206
출처 데이터셋uspto-grants-1989_09
ORD IDord-90131712d2604b749ec11003cd0f12e7
출처 메모uspto-grants-1989_09