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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 388741생성일: 2026년 10월 25일

Methyl morpholine oxide → Hexamethyldisiloxane

https://huagongshe.com/reaction/388741

반응식

참여 물질

역할이름HCID투입량
반응물Methyl morpholine oxideHCID 82029—
반응물(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propan-1-olHCID 15230899—
반응물Trimethyl{[(2s)-1,1,2-trimethyl-3-(phenylsulfonyl)propyl]oxy}silaneHCID 68938726—
촉매HCID 178419074HCID 178419074—
용매DichloromethaneHCID 6344—
생성물HexamethyldisiloxaneHCID 24764—

반응 단계

The compound of Example 10E (200 mg, 0.61 mmol) was dissolved in 2 mL of dichloromethane; 100 mg of 4 Å molecular sieves were added, followed by 15 mg of tetrapropylammonium perruthenate and 75 mg of 4-methylmorpholine N-oxide. The mixture was stirred for 2 hours at ambient temperature, and then filtered through diatomaceous earth to removed solids. The crude product was purified by silica gel chromatography using an Analogix IntelliFlash™ 40, eluting with a gradient of 5% to 30% ethyl acetate in hexanes. The compound of Example 10C (200 mg, 0.63 mmol) was combined with this aldehyde according to the coupling procedure described by Kutner et al. in J. Org. Chem. 1988, 53, 3450-3457. The named product was isolated as a mixture of trimethylsilyl ether (Fraction A) and hydroxyl (Fraction B) after chromatographic purification using an Analogix IntelliFlash 280™, eluting with a gradient of 0% to 50% ethyl acetate in hexanes. These products were combined and carried forward to the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08377913B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-bc265b841cb44c769a0b6e804ede5f28
출처 메모uspto-grants-2013_02