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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11486생성일: 2026년 10월 24일

Methanol → 2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl) ethyl]-N-pentylamide

https://huagongshe.com/ko/reaction/11486

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물TriethylamineHCID 8471—
반응물Oxydiacetyl dichlorideHCID 88769—
반응물2-(1Adamantyl)-n-pentylethylamine hydrochlorideHCID 49831680—
용매DichloromethaneHCID 6344—
생성물2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl) ethyl]-N-pentylamideHCID 5748127360%

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 with ethyl acetate and water (15 ml respectively), 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, the resulting residue was purified by silica gel column chromatography to give 0.39 g (60%) of 2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide as an oily matter.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098226B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-255a07025eca44d1b3ec05d62aa736eb
출처 메모uspto-grants-2006_08