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Methyl morpholine oxide → 5-Phenyl-1H-pyrrole-3-carboxaldehyde
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-Phenyl-1H-pyrrol-3-YL)methanol | HCID 57179302 | — |
| 触媒 | HCID 178419074 | HCID 178419074 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 5-Phenyl-1H-pyrrole-3-carboxaldehyde | HCID 11052090 | 62% |
反応手順
To a solution (45 mL) of (5-phenyl-1H-pyrrol-3-yl)methanol (1.51 g) in acetonitrile were added tetra-n-propylammonium perruthenate (0.46 g), N-methylmorpholine N-oxide (2.36 g) and molecular sieves 4A powder (4.5 g), and the mixture was stirred at room temperature for 1.5 hr. The reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1→1:1) to give the title compound as a pale-yellow powder (yield 0.92 g, 62%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08048909B2 |
| 出典データセット | uspto-grants-2011_11 |
| ORD ID | ord-0624b44e791f4f9688cb18f6e9664367 |
| 出典メモ | uspto-grants-2011_11 |