참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 반응물 | N-methylhydroxylamine hydrochloride | HCID 77906 | — |
| 반응물 | (1,1'-Bi(cyclohexane))-4-carboxylic acid | HCID 3062287 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Sodium Hydroxide | HCID 14798 | — |
| 생성물 | 4-cyclohexyl-N-hydroxy-N-methylcyclohexanecarboxamide | HCID 19835291 | 20.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04889874 |
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| 출처 데이터셋 | uspto-grants-1989_12 |
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| ORD ID | ord-19b7ee22410040a3bdf1d114a7a46b5d |
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| 출처 메모 | uspto-grants-1989_12 |
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