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HRID 477964作成日:2026年10月26日

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

https://huagongshe.com/reaction/477964

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物N-tert-butylhydroxylamine hydrochlorideHCID 2777896—
反応物(1,1'-Bi(cyclohexane))-4-carboxylic acidHCID 3062287—
触媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium HydroxideHCID 14798—
生成物4-cyclohexyl-N-(1,1-dimethylethyl)-N-hydroxy-cyclohexane-carboxamideHCID 147228689.4%

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04889874
出典データセットuspto-grants-1989_12
ORD IDord-81dccbcadc124a5a82208d0bc9af450a
出典メモuspto-grants-1989_12