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Dimethyl Sulfoxide → Cyclohexanepropionaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | 3-Cyclohexyl-1-propanol | HCID 70763 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Sulfur trioxide-pyridine | HCID 168533 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Cyclohexanepropionaldehyde | HCID 78070 | 97.5% |
反応手順
3-Cyclohexyl-1-propanol (3.96 g, 27.8 mmol) was dissolved in DCM (90 mL) at 0° C. and treated sequentially with dimethyl sulfoxide (3.25 g, 41.7 mmol), N,N-diisopropylethylamine (8.98 g, 69.6 mmol) and sulfur trioxide pyridine.complex (11 g, 69.6 mmol). After one hour, the reaction mixture was diluted with DCM (100 mL) and washed with 1N aqueous HCl (3×50 mL), saturated sodium bicarbonate (3×50 mL), and brine. The organic layer was dried over MgSO4, filtered, and concentrated to yield the title intermediate as a light yellow oil (3.8 g). 1H NMR (d6-DMSO, 300 MHz) δ (ppm): 9.72 (s, 1H), 3.65-3.72 (m, 2H), 2.46 (t, 2H), 1.65-1.73 (m, 3H), 1.51-1.56 (m, 2H), 1.14-1.48 (m, 4H), 0.85-0.96 (m, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08664242B2 |
| 出典データセット | uspto-grants-2014_03 |
| ORD ID | ord-c4845d2a92b4461895b1ca8eb893a257 |
| 出典メモ | uspto-grants-2014_03 |