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Salicylaldehyde → 2-[[5-(Acetyloxy)pentyl]oxy]benzaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Salicylaldehyde | HCID 6998 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 5-Bromopentyl acetate | HCID 85140 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 2-[[5-(Acetyloxy)pentyl]oxy]benzaldehyde | HCID 19922112 | 43,549.398% |
反応手順
A mixture of 12.2 g (0.1 mmol) of salicyladehyde, 23 g (0.11 mol) of 5-bromopentyl acetate, 44.2 g (0.3 mol) of anhydrous, granular potassium carbonate, and 700 mL of acetonitrile was stirred and refluxed for 20 hr. After being cooled, the resulting mixture was filtered with suction and the solids were washed well with ether. The filtrate and washes were combined and concentrated in vacuo giving a yellow oil which was purified by flash chromatography on silica gel, eluting with 4:1 hexane-ether. There was obtained 10.9 g (43.6%) of 2-[[5-(acetyloxy)pentyl]oxy]benzaldehyde as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05273999 |
| 出典データセット | uspto-grants-1993_12 |
| ORD ID | ord-96c76a38e9b4404eaa89b1c139393c2e |
| 出典メモ | uspto-grants-1993_12 |