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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132614생성일: 2026년 10월 27일

Ethyl trifluoromethanesulphonate → (4S,5R)-3-((S)-2-Ethyl-pentanoyl)-4-methyl-5-phenyl-oxazolidin-2-one

https://huagongshe.com/reaction/132614

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl trifluoromethanesulphonateHCID 67924—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물(4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-oneHCID 69269495—
용매TetrahydrofuranHCID 8028—
생성물(4S,5R)-3-((S)-2-Ethyl-pentanoyl)-4-methyl-5-phenyl-oxazolidin-2-oneHCID 6926810679%

반응 조건

온도-78 °C

반응 단계

To a −78° C. stirred solution of the (4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-one (9.20 g, 35.2 mmol) in dry THF (150 mL) was added NaHMDS (42.2 mL, 1.0 M in THF) dropwise. After 1 hour, ethyl trifluoromethanesulfonate (5.93 mL, 45.7 mmol) was added dropwise and the reaction was stirred at −78° C. for an additional 2 hours. The reaction was warmed to −30° C. for 30 minutes and quenched with sat. NH4Cl. The layers were separated and the aqueous layer was extracted with EtOAc (3×40 mL). The organic extracts were combined and washed with brine (2×40 mL). The organic phase was dried over MgSO4, filtered, and concentrated under reduced pressure to yield 8.05 g of crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388023B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-207132b15cc3466ba0ff6717cf11d9ed
출처 메모uspto-grants-2008_06