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HRID 231318生成日期:2026年10月23日

聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 3-溴-4-氟苯甲醛

https://huagongshe.com/zh-CN/reaction/231318

反应方程式

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 17360481%

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

DOI10.6084/m9.figshare.5104873.v1
专利号US04845249
来源数据集uspto-grants-1989_07
ORD IDord-dbf6db348254410585d2e7e63a02f66c
来源说明uspto-grants-1989_07