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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1730812생성일: 2026년 10월 25일

Triethylamine → N-cyclohexyl-2,4-dimethylfuran-3-hydroxamic acid

https://huagongshe.com/reaction/1730812

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N-Cyclohexylhydroxylamine hydrochlorideHCID 3084432—
반응물2,4-Dimethyl-3-furoyl chlorideHCID 13019985—
용매BenzeneHCID 241—
생성물N-cyclohexyl-2,4-dimethylfuran-3-hydroxamic acidHCID 21496533—

반응 단계

30 Parts of triethylamine is added to a suspension of 25 parts of N-cyclohexylhydroxylamine hydrochloride in 480 parts of benzene. After the mixture has been stirred for 1 hour, 20 parts of 2,4-dimethylfuran-3-carboxylic chloride is dripped in at room temperature. After the mixture has been stirred for a further 2 hours it is suction filtered, the residue is washed with benzene and the combined benzene phases are washed with water, dried with anhydrous sodium sulfate and evaporated. There is obtained 34 parts of N-cyclohexyl-2,4-dimethylfuran-3-hydroxamic acid in the form of an oil. This oil is dissolved in 370 parts of dichloromethane; at room temperature and while stirring, 18 parts of sodium hydroxide in 70 parts of water, and 28 parts of dimethyl sulfate are added to the solution. After the mixture has been stirred for 1 hour the organic phase is separated, washed with water, dried with sodium sulfate, evaporated and chromatographed using silica gel with a mixture of equal portions of ethyl acetate and cyclohexane. When the eluate is evaporated there is obtained 32 parts of O-methyl-N-cyclohexyl-2,4-dimethylfuran-3-hydroxamic acid having a boiling point at 0.01 mm Hg of 122° to 124° C and the refractive index nD25 : 1.5010. ##SPC13##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03993772
출처 데이터셋uspto-grants-1976_11
ORD IDord-d7ff2d4355894f3cb238b7841a40b25e
출처 메모uspto-grants-1976_11