参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 反应物 | 四氧化硫 | HCID 1118 | — |
| 反应物 | 重铬酸钾 | HCID 24502 | — |
| 反应物 | 3-溴-4-氟苯乙醇 | HCID 2773351 | — |
| 催化剂 | 甲基三辛基氯化铵 | HCID 21218 | — |
| 溶剂 | 二氯甲烷 | HCID 6344 | — |
| 产物 | 3-溴-4-氟苯甲醛 | HCID 173604 | 81% |
反应步骤
A misture of 29.4 g (0.3 mol) of sulphuric acid, 50 ml of water and 2 ml of Aliquat 336 (tricapryl-methyl-ammonium chloride) was added to a solution of 20.5 g (0.1 mol) of 3-bromo-4-fluoro-benzyl alcohol in 250 ml of methylene chloride at room temperature. Thereafter, 9.7 g (0.033 mol) of potassium dichromate were added to the reaction mixture and the temperature was kept at about 25° C. for 2 hours by cooling slightly. After adding 100 ml of water, the organic phase was separated off and the aqueous phase was extracted once more with 100 ml of methylene chloride. The organic phases were washed twice with 100 ml of water each time, then once with 100 ml of saturated sodium bicarbonate solution and once more with 100 ml of water, dried over sodium sulphate and evaporated in vacuo. The residue was distilled. 16.3 g (81% of theory) of 3-bromo-4-fluoro-benzaldehyde were obtained in this manner as a colorless oil with a boiling point of 65° C./0.3 mm Hg.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US04845249 |
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| 来源数据集 | uspto-grants-1989_07 |
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| ORD ID | ord-dbf6db348254410585d2e7e63a02f66c |
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| 来源说明 | uspto-grants-1989_07 |
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