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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477963생성일: 2026년 10월 25일

Oxalyl chloride → 4-cyclohexyl-N-hydroxy-N-methylcyclohexanecarboxamide

https://huagongshe.com/reaction/477963

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물N-methylhydroxylamine hydrochlorideHCID 77906—
반응물(1,1'-Bi(cyclohexane))-4-carboxylic acidHCID 3062287—
촉매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Sodium HydroxideHCID 14798—
생성물4-cyclohexyl-N-hydroxy-N-methylcyclohexanecarboxamideHCID 1983529120.4%

반응 단계

To a solution of 4-cyclohexyl-cyclohexanecarboxylic acid (1.47 g, 7 mmol) in 50 ml of tetrahydrofuran was added oxalyl chloride (0.67 ml, 7.7 mmol) and a few drops of dimethylformamide. After stirring for one hour, the reaction mixture was concentrated to about 1/3 of the original volume and added dropwise into a cold (~0° C.), stirred solution of N-methylhydroxylamine hydrochloride (1.17 g, 14 mmol) in 40 ml of 1N sodium hydroxide. The mixture was stirred for two hours and extracted three times with ethyl acetate. The combined ethyl acetate extracts were washed twice with water, dried with anhydrous sodium sulfate and concentrated. Purification by flash chromatography and crystallization afforded 0.342 g of 4-cyclohexyl-N-hydroxy-N-methylcyclohexanecarboxamide as a white solid (m.p. 89°-90° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04889874
출처 데이터셋uspto-grants-1989_12
ORD IDord-19b7ee22410040a3bdf1d114a7a46b5d
출처 메모uspto-grants-1989_12