Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18415생성일: 2026년 10월 26일
Methanol → 2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl) ethyl]-N-pentylamide
https://huagongshe.com/reaction/18415
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Oxydiacetyl dichloride | HCID 88769 | — |
| 반응물 | 2-(1Adamantyl)-n-pentylethylamine hydrochloride | HCID 49831680 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl) ethyl]-N-pentylamide | HCID 57481273 | 60% |
반응 단계
2-(1-Adamantyl)-N-pentylethylamine hydrochloride (Intermediate No. 1-1, 0.50 g, 1.7 mmol) was added to a solution of diglycolyl chloride (0.31 ml, 2.6 mmol) and triethylamine (0.70 ml, 5.1 mmol) in anhydrous dichloromethane (6 ml) under ice-cooling, and the mixture was stirred at room temperature overnight. Methanol (5 ml) was added to the reaction mixture, and the whole was stirred for three hours. The solvent was evaporated under reduced pressure, the residue was distributed between ethyl acetate (15 ml) and water (15 ml), and the organic layer was washed with a saturated aqueous sodium chloride solution (5 ml) and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography to give 2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl)ethyl]-1-pentylamide (0.39 g, 60%) as an oily matter.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07741346B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-fb8549f412814648ab7a6e6616864d3a |
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| 출처 메모 | uspto-grants-2010_06 |
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