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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 655725생성일: 2026년 10월 26일

Magnesium trifluoromethanesulfonate → (R)-methyl 2-hydroxy-3-((S)-1-(triisopropylsilyloxy)propan-2-yloxy)propanoate

https://huagongshe.com/reaction/655725

반응식

참여 물질

역할이름HCID투입량
반응물Magnesium trifluoromethanesulfonateHCID 2734125—
반응물Methyl (2R)-2-oxiranecarboxylateHCID 9877347—
반응물(S)-1-(triisopropylsilyloxy)propan-2-olHCID 57504699—
용매Ethyl AcetateHCID 8857—
생성물(R)-methyl 2-hydroxy-3-((S)-1-(triisopropylsilyloxy)propan-2-yloxy)propanoateHCID 8664084741.2%

반응 조건

온도80 °C

반응 단계

Magnesium trifluoromethanesulfonate (1.263 g, 3.92 mmol) was added to a mixture of (S)-1-(triisopropylsilyloxy)propan-2-ol (4.55 g, 19.59 mmol) and (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) in ethyl acetate (40 mL). The resulting suspension was heated to 80° C. for 72 hours. Further (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) was added and the mixture stirred at 80° C. for 48 hrs. Further (R)-methyl oxirane-2-carboxylate (2 g, 19.59 mmol) was added and the mixture stirred for 24 hrs. The mixture was allowed to cool, filtered through a bed of silica (˜10 g), washed through with EtOAc and evaporated. The crude product was purified by flash silica chromatography, elution gradient 10 to 50% EtOAc in isohexane, to afford the product (2.7 g, 41%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071608B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-786616f159c04a1491d48599f08480bf
출처 메모uspto-grants-2011_12