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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477964생성일: 2026년 10월 25일

Oxalyl chloride → 4-cyclohexyl-N-(1,1-dimethylethyl)-N-hydroxy-cyclohexane-carboxamide

https://huagongshe.com/reaction/477964

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물N-tert-butylhydroxylamine hydrochlorideHCID 2777896—
반응물(1,1'-Bi(cyclohexane))-4-carboxylic acidHCID 3062287—
촉매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Sodium HydroxideHCID 14798—
생성물4-cyclohexyl-N-(1,1-dimethylethyl)-N-hydroxy-cyclohexane-carboxamideHCID 147228689.4%

반응 단계

To a solution of 4-cyclohexyl-cyclohexanecarboxylic acid (1.47 g, 7 mmol) in 20 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 added dropwise into a cold (~0° C.), stirred solution of N-(1,1-dimethylethyl)hydroxylamine hydrochloride (1.75 g, 14 mmol) in 40 ml of 1N sodium hydroxide. The mixture was stirred for two hours, from 0° C. to room temperature and extracted three times with ethyl acetate. The combined ethyl acetate extracts were then washed twice with water, dried with anhydrous sodium sulfate and concentrated. Purification by flash chromatography provided 0.186 g of the 4-cyclohexyl-N-(1,1-dimethylethyl)-N-hydroxy-cyclohexane-carboxamide as a white solid (m.p. 119°-120° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04889874
출처 데이터셋uspto-grants-1989_12
ORD IDord-81dccbcadc124a5a82208d0bc9af450a
출처 메모uspto-grants-1989_12