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Acetic Acid → 5-[(1,5-Dimethylhexyl)oxy]pentanal
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | {4-[(1,5-Dimethylhexyl)oxy]butyl}-1,3-dioxolane | HCID 66623666 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 5-[(1,5-Dimethylhexyl)oxy]pentanal | HCID 86642023 | 26% |
反応手順
{4-[(1,5-dimethylhexyl)oxy]butyl}-1,3-dioxolane (1.4 g, 43% pure by GC RPA, 3.9 mmol), acetic acid (10 mL), tetrahydrofuran (16 mL) and water (20 mL) were added to a 100 mL three-necked flask fitted with thermocouple, magnetic stirrer and condenser. The reaction mixture was refluxed for 2 hrs, cooled and saturated sodium carbonate (150 mL) added. The crude reaction mixture was extracted with hexane (4×100 mL), the combined organic phase dried over magnesium sulphate, filtered and the solvent removed in vacuo. The crude product was chromatographed over silica gel (hexane/methyltert-butyl ether) to yield pure 5-[(1,5-dimethylhexyl)oxy]pentanal as a colourless oil (0.22 g, 1.02 mmol, chemical yield 26%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08088725B2 |
| 出典データセット | uspto-grants-2012_01 |
| ORD ID | ord-a124b7fabb02462cb655ee245bf1f3b1 |
| 出典メモ | uspto-grants-2012_01 |