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HRID 66637作成日:2026年10月25日

Sodium Chloride → HCID 178490609、化合物

https://huagongshe.com/reaction/66637

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物Sodium CyanideHCID 8929—
反応物Acetonitrile, fluoro-HCID 10420—
反応物Ammonium ChlorideHCID 25517—
反応物2-(Benzyloxy)-4-(chloromethyl)-1-methoxybenzeneHCID 280224—
反応物MagnesiumHCID 5462224—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178490609HCID 178490609—

反応条件

温度-30 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04342780
出典データセットuspto-grants-1982_08
ORD IDord-a3ef8b34366e4a66a317bdcc6edb8c68
出典メモuspto-grants-1982_08