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HRID 48128생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/48128

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Methyl nitriteHCID 12231—
반응물Sodium HydroxideHCID 14798—
반응물Sodium NitriteHCID 23668193—
반응물4-(4-Methylphenyl)but-3-enenitrileHCID 57119144—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Methanol--water (1/1)HCID 22242641—
생성물2-Hydroxyimino-4-p-tolyl-but-3-enenitrileHCID 8675935776%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703182B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-d0543945a5a8420b92d3a782a42edabb
출처 메모uspto-grants-2004_03