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HRID 16211作成日:2026年10月25日

Methyl morpholine oxide → 5-(Tert-butyldimethylsilyloxy)cyclooctanone

https://huagongshe.com/reaction/16211

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5-(tert-Butyl-dimethyl-silanyloxy)-cyclooctanolHCID 14321678—
触媒HCID 178419074HCID 178419074—
溶媒DichloromethaneHCID 6344—
生成物5-(Tert-butyldimethylsilyloxy)cyclooctanoneHCID 10978090—

反応手順

Tetrapropylammonium perruthenate (0.82 g, 2.43 mmol) was added to a stirred and cooled (0° C.) solution of Example 5A (12.11 g, 46.90 mmol), 4-methylmorpholine N-oxide (8.24 g, 70.35 mmol), and 4 Å molecular sieves (23 g) in dry dichloromethane (120 mL). After the addition, the mixture was warmed to room temperature and stirred for another three hours. The black mixture was filtered through a pad of Celite and the solvent was evaporated. The residue was purified over silica gel using 5-50% ethyl acetate in hexanes to give the title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737137B2
出典データセットuspto-grants-2010_06
ORD IDord-15ceb4157b1d41a3b0c06c610f11091f
出典メモuspto-grants-2010_06