돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218018생성일: 2026년 10월 25일

Methanol → Methyl 3-aminoadamantane-1-carboxylate hydrochloride

https://huagongshe.com/reaction/218018

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Thionyl ChlorideHCID 24386—
반응물3-Aminoadamantane-1-carboxylic acid hydrochlorideHCID 365220—
생성물Methyl 3-aminoadamantane-1-carboxylate hydrochlorideHCID 285288692%

반응 조건

온도60 °C

반응 단계

To a 3-neck 2-L flask equipped with a reflux condenser and a temperature probe was added 3-amino-adamantane-1-carboxylic acid hydrochloride (100 g, 432 mmol) and methanol (1.0 L). To this solution was slowly added thionyl chloride (15.7 mL, 216 mmol) and the reaction was heated at 60° C. for 4 hours. Once cooled to room temperature, the crude reaction mixture was concentrated under reduced pressure to remove most of the methanol. Heptane (about 1-L) was then added and the mixture was once again concentrated under reduced pressure at which point a solid began to precipitate. This process was repeated three more times, then the solids were filtered off, washed with heptane and allowed to dry in open air to afford 97.2 g (92%) of the title compound, 3-amino-adamantane-1-carboxylic acid methyl ester hydrochloride, as a white solid. 1H NMR (300 MHz, CDCl3) δ 8.46 (br s, 3H), 3.65 (s, 3H), 2.33-2.24 (m, 2H), 2.23-2.16 (m, 2H), 2.11-1.95 (m, 4H), 1.94-1.78 (m, 4H), 1.75-1.62 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198275B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-9ec47c4cf75c4e27b8c7d5ba57be580d
출처 메모uspto-grants-2012_06