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HRID 388741作成日:2026年10月25日

Methyl morpholine oxide → Hexamethyldisiloxane

https://huagongshe.com/reaction/388741

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl morpholine oxideHCID 82029—
反応物(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propan-1-olHCID 15230899—
反応物Trimethyl{[(2s)-1,1,2-trimethyl-3-(phenylsulfonyl)propyl]oxy}silaneHCID 68938726—
触媒HCID 178419074HCID 178419074—
溶媒DichloromethaneHCID 6344—
生成物HexamethyldisiloxaneHCID 24764—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08377913B2
出典データセットuspto-grants-2013_02
ORD IDord-bc265b841cb44c769a0b6e804ede5f28
出典メモuspto-grants-2013_02