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Dimethyl Sulfoxide → 5-Methanesulfonylpentanal
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | 5-Methanesulfonylpentan-1-ol | HCID 23028699 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | 5-Methanesulfonylpentanal | HCID 23028565 | 54% |
反応手順
To a dichloromethane (15 ml) solution of 5-(methylsulfonyl)-1-pentanol (344 mg, 2.07 mmol), dimethylsulfoxide (0.441 ml, 6.21 mmol) and triethylamine (1.15 ml, 8.28 ml) was added a sulfur trioxide pyridine complex (659 mg, 4.14 mmol) at 0° C. and the mixture was stirred at room temperature for 3 hours. After the reaction mixture was washed with water, the organic layer was dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was subjected to flash silica gel chromatography, and the fraction obtained from the ethyl acetate eluate was concentrated under reduced pressure, whereby the title compound (183 mg, 1.11 mmol, 54%) was obtained as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07399775B2 |
| 出典データセット | uspto-grants-2008_07 |
| ORD ID | ord-9b5dab2b43f74bfcb8584aec2f045974 |
| 出典メモ | uspto-grants-2008_07 |