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ChemicalBook CAS DataBase List 4-ETHYNYLBENZALDEHYDE

4-ETHYNYLBENZALDEHYDE synthesis

9synthesis methods
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Yield:63697-96-1 85.1%

Reaction Conditions:

Stage #1:4-bromo-benzaldehyde with triethylamine in tetrahydrofuran for 0.75 h;Inert atmosphere;
Stage #2:trimethylsilylacetylene with copper(l) iodide;triphenylphosphine hydrochloride in tetrahydrofuran for 10 h;Inert atmosphere;
Stage #3: with potassium carbonate in methanol at 20; for 5 h;

Steps:

1.3.a; 1.3.b
15.0 mmol (2.78 g) of p-bromobenzaldehyde was dissolved in 95 ml of a tetrahydrofuran and triethylamine mixed solution (1: 1 by volume) and placed in a 250 ml single-necked flask,The cells were ventilated for 45 minutes and then 18.0 mmol (1.76 g)Of trimethylsilylacetylene. Adding 97.2 mg of triphenylphosphonium dichloride,46.5mg cuprous iodide. Under argon, the reaction was carried out for 10 hours.After the reaction was stopped, the solvent was removed by distillation under reduced pressure and purified by silica gel column chromatography (developing solvent: dichloromethane: petroleum ether 1: 4), steamed and dried in vacuo to give 2.19 g of a white solid in 72.3% yield.B: A solution of 8.0 mmol (1.62 g) of a product was dissolved in 30 mlMethanol and 60 ml of tetrahydrofuran, placed in a 250 ml single-necked round bottom flask,Then add anhydrous potassium carbonate,And the mixture was stirred at room temperature for 5 hours. The solvent was distilled off under reduced pressure,Silica gel column (developing solvent for petroleum ether and dichloromethane 1: 1 mixed solvent) crude purification;Dried in vacuo to give 0.88 g of a white solid in 85.1%

References:

Xijing College;Zhao Yuzhen;Miao Zongcheng;Li Kexuan;Lin Dong;Ren Huaping;Zhu Min;Liu Kun CN106588789, 2017, A Location in patent:Paragraph 0047-0049

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