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Methyl morpholine oxide → 5-(Tert-butyldimethylsilyloxy)cyclooctanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl morpholine oxide | HCID 82029 | — |
| 反応物 | 5-(tert-Butyl-dimethyl-silanyloxy)-cyclooctanol | HCID 14321678 | — |
| 触媒 | HCID 178419074 | HCID 178419074 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5-(Tert-butyldimethylsilyloxy)cyclooctanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07737137B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-15ceb4157b1d41a3b0c06c610f11091f |
| 出典メモ | uspto-grants-2010_06 |