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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1070038생성일: 2026년 10월 25일

Isoamyl Nitrite → 2-Hydroxyimino-2-(3-phenoxyphenyl)acetonitrile

https://huagongshe.com/reaction/1070038

반응식

참여 물질

역할이름HCID투입량
반응물Isoamyl NitriteHCID 8053—
반응물m-Phenoxybenzyl cyanideHCID 40075—
반응물Sodium ethoxideHCID 2723922—
반응물SodiumHCID 5360545—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
생성물2-Hydroxyimino-2-(3-phenoxyphenyl)acetonitrileHCID 8530827945%

반응 단계

To a solution of sodium ethoxide prepared from sodium (1.09 g) and ethanol (20 ml), a solution of 3-phenoxyphenylacetonitrile (8.30 g) in ethanol (15 ml) was added dropwise at 0° C., and then isoamyl nitrite (7.99 ml) was added dropwise. After stirring for 15 hours at room temperature, diethyl ether was added and the mixture was washed sequentially with 1N HCl, aqueous sodium bicarbonate and then saturated aqueous sodium chloride. The diethyl ether layer was dried (MgSO4), concentrated, and the residue was subjected to column chromatography on silica gel. The crystals obtained from a fraction eluted with ethyl acetate-hexane (1:4, v/v) were recrystallized with ethyl acetate-hexane to obtain 2-hydroxyimino-2-(3-phenoxyphenyl)acetonitrile (4.25 g, yield: 45%) as pale-yellow crystals. A mixture of the E- form and the Z- form. m.p. 124-125° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06251926B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-4315ba764d5148efaf6776f8b73e386d
출처 메모uspto-grants-2001_06