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Cornforth reagent → Spiro(2.5)octane-6-carbaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Cornforth reagent | HCID 2724130 | — |
| 反応物 | (Spiro(2.5)octan-6-yl)methanol | HCID 53487089 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Spiro(2.5)octane-6-carbaldehyde | HCID 86598198 | — |
反応手順
Spiro[2.5]oct-6-yl-methanol (2.57 g, 18.3 mmol, 1.0 eq.) was dissolved in CH2Cl2 (30 mL) and placed in a ice-water bath at 0° C. Pyridinium dichromate (PCC) (7.9 g, 36.6 mmol, 2.0 eq.) was added and the reaction warmed to room temperature for 4 hours with stirring. The crude reaction was filtered through a Celite pad and washed with CH2Cl2 and evaporated. The crude material was dissolved in diethyl ether and filtered through Celite, washing with diethyl ether several times. Evaporated solvent to provide Spiro[2.5]octane-6-carbaldehyde as a brown oil (2.98 g, quantitative) that was used directly. 1H NMR (CHCl3, 400 MHz) δ 0.17-0.27 (m, 4H), 0.88-0.91 (m, 2H), 1.09-1.25 (m, 2H), 1.52-1.54 (m, 2H), 1.69-1.75 (m, 3H), 9.44 (d, 1H, J=1.2 Hz).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07501408B2 |
| 出典データセット | uspto-grants-2009_03 |
| ORD ID | ord-98383634377349609046a0d1ae6cb608 |
| 出典メモ | uspto-grants-2009_03 |