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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66637생성일: 2026년 10월 24일

Sodium Chloride → HCID 178490609, 화합물

https://huagongshe.com/ko/reaction/66637

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Sodium CyanideHCID 8929—
반응물Acetonitrile, fluoro-HCID 10420—
반응물Ammonium ChlorideHCID 25517—
반응물2-(Benzyloxy)-4-(chloromethyl)-1-methoxybenzeneHCID 280224—
반응물MagnesiumHCID 5462224—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물HCID 178490609HCID 178490609—

반응 조건

온도-30 °C

반응 단계

Under an atmosphere of nitrogen, 3-benzyloxy-4-methoxybenzyl magnesium chloride is prepared from 3-benzyloxy-4-methoxybenzylchloride (C. Schopf and L. Winterhalder, Ann. 544, 62 (1940) (22.0 g, 84 mmol) and magnesium turnings (4.1 g) in tetrahydrofuran (THF) (100 ml) at room temperature (about 2 hours). After cooling to -30° C., a solution of fluoroacetonitrile (4.94 g) in THF (40 ml) is added dropwise, maintaining the temperature between -30° C. and -40° C. Stirring is continued at this temperature for another 30 minutes, then the mixture is poured into a solution of sodium cyanide (12.3 g) and ammonium chloride (17.9 g) in water (150 ml), previously cooled with ice. After stirring for 30 minutes, the mixture is saturated with sodium chloride whereupon the phases separate. After extracting the aqueous phase two more times with diethyl ether, the combined THF and ether phases are dried (Na2SO4) and evaporated to give the crude aminonitrile (25.9 g) as a brown oil. The oil is dissolved in ether and treated with HCl gas to prepare the hydrochloride as an oil. This oil is recrystallized twice from ethanol/ether to give 2-fluoromethyl-2-amino-3-(3'-benzyloxy-4'-methoxyphenyl)propionitrile as the hydrochloride as a slightly colored solid; NMR (CD3OC): 3.47 ppm (3H, s), 4.32 ppm (2H, d, JH--F =46 Hz), 4.73 ppm (2H, s), 6.60 ppm (3H, m), 6.97 ppm (5H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04342780
출처 데이터셋uspto-grants-1982_08
ORD IDord-a3ef8b34366e4a66a317bdcc6edb8c68
출처 메모uspto-grants-1982_08