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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 612348생성일: 2026년 10월 24일

Water → (4-Methylsulfonyloxyimino-cyclohexa-2,5-dienylidene)-phenyl-acetonitrile

https://huagongshe.com/ko/reaction/612348

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물2-(4-(Hydroxyimino)cyclohexa-2,5-dien-1-ylidene)-2-phenylacetonitrileHCID 346833—
용매TetrahydrofuranHCID 8028—
생성물(4-Methylsulfonyloxyimino-cyclohexa-2,5-dienylidene)-phenyl-acetonitrileHCID 2218419570%

반응 단계

10 g (45 mmol) of (4-Hydroxyimino-cyclohexa-2,5-dienylidene)-phenyl-acetonitrile are dissolved in 100 ml of tetrahydrofuran (THF) and cooled in an ice bath. After adding 9.41 ml (68 mmol) of triethylamine to the solution, 3.83 ml (50 mmol) of methanesulfonyl chloride are added dropwise, keeping the temperature below 5° C. The reaction mixture is gradually warmed to room temperature, and stirred for 1 hr. The reaction mixture is poured into 200 ml of water, and extracted with ethyl acetate. The organic phase is washed with hydrochloric acid solution, water, and sodium chloride solution. The organic phase is dried over MgSO4, the solvent is distilled off, and the residue is purified by recrystallization from toluene. 9.4 g (70%) of (4-Methylsulfonyloxyimino-cyclohexa-2,5-dienylidene)-phenyl-acetonitrile are obtained in the form of a yellow-green crystal having a melting point of 137-139° C. (dec.). 1H-NMR shows that the product is a 82:18 mixture of the E and Z isomers (two dxd signals for H-C(2 or 6) at 6.78 and 6.91 ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06004724
출처 데이터셋uspto-grants-1999_12
ORD IDord-d3822b41411a457ca102026d4824804d
출처 메모uspto-grants-1999_12