反应 #4135501
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2e45375f6d5b4b2d9d01ed464c21645a暂无可渲染的结构数据
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乙基3-氰基-3-苯丙酸酯(CAS 14025-83-3)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2e45375f6d5b4b2d9d01ed464c21645a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4353e4cb4b144508baba9bca531b3e8c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-058e9fbd6ae949b79c29bb35dab4681f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2e45375f6d5b4b2d9d01ed464c21645a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2e45375f6d5b4b2d9d01ed464c21645a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4353e4cb4b144508baba9bca531b3e8c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4353e4cb4b144508baba9bca531b3e8c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 120 g of benzalmalonic acid diethyl ester, 33.6 g of potassium cyanide, 1600 cc of ethanol and 160 cc of water are stirred at a bath temperature of 60° for 12 to 14 hours. The reaction mixture is then cooled with ice water, the potassium bicarbonate which crystallizes is filtered off, the filtrate is made neutral with about 15 cc of 1 N hydrochloric acid, air is passed through the solution with a water jet vacuum pump for 1 hour, the solvent is distilled off on a rotary evaporator, 100 cc of water are added to the oily residue, and extraction is effected 6 times with 250 cc amounts of ether. The 3-cyano-3-phenyl-propionic acid ethyl ester, obtained after distilling off the ether, is purified by vacuum distillation. B.P. 125°-130°/0.15 mm Hg. the potassium bicarbonate which crystallizes is filtered off the solvent is distilled off on a rotary evaporator, 100 cc of water are added to the oily residue, and extraction
来源 ID: ord-d6029a477334409b996241ed14078935反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 43.5 g (214 mmol) of ethyl 3-cyano-3-phenylpropanoate and 52.2 g (930.4 mmol) of potassium hydroxide in 670 mL of EtOH is refluxed for 4 hours. After cooling to room temperature, the medium is concentrated under vacuum and then treated with 1 L of 1N HCl, and a precipitate then forms, which is filtered off and rinsed with water (2×50 mL). The solid obtained is taken up in a mixture of 200 mL of toluene and 40 mL of EtOH and concentrated under reduced pressure, and then dried with a vane pump. 37 g of 2-phenylbutanedioic acid are obtained in the form of a solid, which is used without further purification in the following step. is refluxed for 4 hours the medium is concentrated under vacuum treated with 1 L of 1N HCl which is filtered off rinsed with water (2×50 mL) The solid obtained concentrated under reduced pressure dried with a vane pump
来源 ID: ord-9606fc799fc148db8f11487efd069dc2反应条件: temp:60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 64 g (257.8 mmol) of diethyl benzylidenepropanedioate and 17 g (261 mmol) of potassium cyanide in 750 mL of EtOH and 75 mL of water is heated for 18 hours at 60° C. The medium is then concentrated under reduced pressure and taken up in 500 mL of brine and then extracted with Et2O (2×500 mL). The organic phases are dried over Na2SO4, filtered and then concentrated under reduced pressure. 43.5 g of ethyl 3-cyano-3-phenylpropanoate are obtained in the form of a solid, which is used without further purification in the following step. The medium is then concentrated under reduced pressure extracted with Et2O (2×500 mL) The organic phases are dried over Na2SO4 filtered concentrated under reduced pressure
来源 ID: ord-5573ee57bf374732b420222de8048606反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-058e9fbd6ae949b79c29bb35dab4681f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 43.5 g (214 mmol) of ethyl 3-cyano-3-phenylpropanoate and 52.2 g (930.4 mmol) of potassium hydroxide in 670 mL of EtOH is refluxed for 4 hours. After cooling to room temperature, the medium is concentrated under vacuum and then treated with 1 L of 1N HCl, and a precipitate then forms, which is filtered off and rinsed with water (2×50 mL). The solid obtained is taken up in a mixture of 200 mL of toluene and 40 mL of EtOH and concentrated under reduced pressure, and then dried with a vane pump. 37 g of 2-phenylbutanedioic acid are obtained in the form of a solid, which is used without further purification in the following step. is refluxed for 4 hours the medium is concentrated under vacuum treated with 1 L of 1N HCl which is filtered off rinsed with water (2×50 mL) The solid obtained concentrated under reduced pressure dried with a vane pump
来源 ID: ord-9606fc799fc148db8f11487efd069dc2PubChem References
以下资料来自该化合物的公开数据库参考记录。
