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HRID 48128作成日:2026年10月25日

Sulfuric Acid → 2-Hydroxyimino-4-p-tolyl-but-3-enenitrile

https://huagongshe.com/reaction/48128

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Methyl nitriteHCID 12231—
反応物Sodium HydroxideHCID 14798—
反応物Sodium NitriteHCID 23668193—
反応物4-(4-Methylphenyl)but-3-enenitrileHCID 57119144—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Methanol--water (1/1)HCID 22242641—
生成物2-Hydroxyimino-4-p-tolyl-but-3-enenitrileHCID 8675935776%

反応条件

温度0 °C

反応手順

In a 3-necked 50 ml flask fitted with a sintered glass gas inlet tube, 2.13 g (0.0135 mol) of 4-p-tolyl-but-3-enenitrile are dissolved in 30 ml of methanol, and cooled to 0° C. Sodium hydroxide (0.54 g; 0.0135 mol) is added. The turbid, slightly brownish mixture is then treated with ca. 0.025 mol of gaseous methyl nitrite bubbled below the surface of the mixture through the gas inlet tube (methyl nitrite is generated by dropwise addition of [0.8 ml of H2SO4 conc+1.6 ml H2O] to a suspension of sodium nitrite (1.72 g; 0.025 mol) in 3 ml of methanol:water 1:1 (v:v); see M. Itoh et al. Org. Synth. Coll vol. VI, 1988, 199). The mixture is then stirred overnight, allowing the temperature to rise to 25° C. The solvent is evaporated in vacuo, the residue is redissolved in water and extracted with toluene. The aqueous phase is then acidified with conc. HCl to pH ca 2, the beige precipitate is filtered, rinsed neutral with water, and dried under vacuum. The crude product is redissolved in ethyl acetate, filtered through a short pad of SiO2, and evaporated. 2-Hydroxyimino-4-p-tolyl-but-3-enenitrile (1.9 g; 76%), mp 135-137° C. is obtained and used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703182B1
出典データセットuspto-grants-2004_03
ORD IDord-d0543945a5a8420b92d3a782a42edabb
出典メモuspto-grants-2004_03