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HRID 466041作成日:2026年10月26日

Hydrazine → HCID 178496297、化合物

https://huagongshe.com/reaction/466041

反応式

関与物質

役割名称HCID仕込み量
反応物HydrazineHCID 9321—
反応物Sodium hydrideHCID 24758—
反応物Sodium BicarbonateHCID 516892—
反応物3,5-Bis(1,1-dimethylethyl)-4-[(2-methoxyethoxy)methoxy]benzonitrileHCID 10041643—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178496297HCID 17849629767%

反応条件

温度0 °C

反応手順

97% anhydrous hydrazine (4.8 g, 0.151 mole) is added dropwise to a stirred 0° C. suspension of sodium hydride (2.8 g of a 60% dispersion in mineral oil, 0.071 mol) in tetrahydrofuran (70 m) under nitrogen. After 90 minutes, a solution of 3,5-bis(1,1-dimethylethyl)-4-[(2-methoxyethoxy)methoxy]benzonitrile (6.7 g, 0.021 mole) in tetrahydrofuran (15 ml) is added dropwise. After stirring two hours at 0° C., water 2.4 ml) is added dropwise. The mixture is poured into cold, saturated aqueous sodium bicarbonate 20 ml). The product is extracted with a 1:1 ethyl acetate/ether mixture (60 ml). The organic layer is washed with saturated aqueous NaCl and dried over MgSO4. Filtration and concentration provided a solid which was recrystallized from ethyl acetate/hexane to give 4.9 g (7.3 g theor., 67%) of 3,5-bis(1,1-dimethylethyl)-4-[(2-methoxyethoxy)methoxy]benzene carboximidic acid hydrazide, mp 133° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05155122
出典データセットuspto-grants-1992_10
ORD IDord-62dcd841198a4b69b96afab4839a93aa
出典メモuspto-grants-1992_10