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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,2-Dimethoxypropane | HCID 6495 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | N-Boc-L-serine methyl ester | HCID 7019177 | — |
| 촉매 | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 3-tert-Butyl 4-methyl 2,2-dimethyl-1,3-oxazolidine-3,4-dicarboxylate | HCID 5138497 | 117.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08093395B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-ecb94918a35e424aba8e681fc8c7aea2 |
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| 출처 메모 | uspto-grants-2012_01 |
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