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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 419758생성일: 2026년 10월 27일

2,2-Dimethoxypropane → 3-tert-Butyl 4-methyl 2,2-dimethyl-1,3-oxazolidine-3,4-dicarboxylate

https://huagongshe.com/reaction/419758

반응식

참여 물질

역할이름HCID투입량
반응물2,2-DimethoxypropaneHCID 6495—
반응물Sodium BicarbonateHCID 516892—
반응물N-Boc-L-serine methyl esterHCID 7019177—
촉매Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
용매BenzeneHCID 241—
생성물3-tert-Butyl 4-methyl 2,2-dimethyl-1,3-oxazolidine-3,4-dicarboxylateHCID 5138497117.5%

반응 단계

Commercially available N-tert-butoxycarbonyl-serine methyl ester (2.0 g, 9.122 mmol), 2,2-dimethoxypropane (1.9 g, 18.24 mmol), and pyridinium-p-toluene sulfonate (26 mg, 137 μmol) were dissolved in benzene (29 ml) and heated under reflux for 15 hours. A saturated sodium hydrogen carbonate solution was added to the reaction mixture, and the mixture was extracted with diethylether; the organic layer was subsequently washed with a saturated sodium chloride solution. The washed product was then dried over anhydrous magnesium sulfate and filtered, and the filtrate was subsequently concentrated. The resulting concentrate was purified by silica gel column chromatography to produce 3-tert-butyl 4-methyl 2,2-dimethyloxazolidine-3,4-dicarboxylate (2.78 g, 91% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093395B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-ecb94918a35e424aba8e681fc8c7aea2
출처 메모uspto-grants-2012_01