反应 #4167297
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-55c385b2d83f4590ad4e2701095f9b42暂无可渲染的结构数据
C1=CC=C(C=C1)CC(=O)C2=CC=CC=C2N产品信息
Ethanone, 1-(2-aminophenyl)-2-phenyl-(CAS 835-38-1)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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9 条反应 · 9 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-55c385b2d83f4590ad4e2701095f9b42反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f37d5de2dacd40018b33ce7bfc019fca反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-55c385b2d83f4590ad4e2701095f9b42反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f37d5de2dacd40018b33ce7bfc019fca反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2-aminobenzonitrile (4.25 g, 36 mmol) in anhydrous diethyl ether (40 ml) at 0° C. is treated under argon with benzylmagnesium chloride (2M in tetrahydrofuran; 50 ml; 100 mmol). The reaction medium is maintained under agitation for 1 hour at ambient temperature, then hydrolyzed at 0° C. by adding hydrochloric acid at 10%, agitated for 1 hour, and neutralized with soda. The resulting mixture is extracted with ethyl acetate. The combined extracts are washed with water and with a saturated solution of sodium chloride, then dried over magnesium sulphate and concentrated to produce 3.5 g of the desired product, in the form of a white solid (m.p.: 100–101° C.). hydrolyzed at 0° C. The resulting mixture is extracted with ethyl acetate The combined extracts are washed with water and with a saturated solution of sodium chloride dried over magnesium sulphate concentrated
来源 ID: ord-4a4a49a3ce5c4056b46634c5b240a433反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2-aminobenzonitrile (4.25 g, 36 mmol) in anhydrous diethyl ether (40 ml) at 0° C. is treated under argon with benzylmagnesium chloride (2M in tetrahydrofuran; 50 ml; 100 mmol). The reaction medium is maintained under agitation for 1 hour at ambient temperature, then hydrolyzed at 0° C. by adding hydrochloric acid at 10%, agitated for 1 hour, and neutralized with soda. The resulting mixture is extracted with ethyl acetate. The combined extracts are washed with water and with a saturated solution of sodium chloride, then dried over magnesium sulphate and concentrated to produce 3.5 g of the desired product, in the form of a white solid (m.p.: 100-101° C). hydrolyzed at 0° C. The resulting mixture is extracted with ethyl acetate The combined extracts are washed with water and with a saturated solution of sodium chloride dried over magnesium sulphate concentrated
来源 ID: ord-76ca4682e42a4d088ec5291911f05da8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2-aminobenzonitrile (4.25 g, 36 mmol) in anhydrous diethyl ether (40 ml) at 0° C. is treated under argon with benzylmagnesium chloride (2M in tetrahydrofuran; 50 ml; 100 mmol). The reaction medium is maintained under agitation for 1 hour at ambient temperature, then hydrolyzed at 0° C. by adding hydrochloric acid at 10%, agitated for 1 hour, and neutralized with soda. The resulting mixture is extracted with ethyl acetate. The combined extracts are washed with water and with a saturated solution of sodium chloride, then dried over magnesium sulphate and concentrated to produce 3.5 g of the desired product, in the form of a white solid (m.p.: 100-101° C). hydrolyzed at 0° C. The resulting mixture is extracted with ethyl acetate The combined extracts are washed with water and with a saturated solution of sodium chloride dried over magnesium sulphate concentrated
来源 ID: ord-76ca4682e42a4d088ec5291911f05da8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2-aminobenzonitrile (4.25 g, 36 mmol) in anhydrous diethyl ether (40 ml) at 0° C. is treated under argon with benzylmagnesium chloride (2M in tetrahydrofuran; 50 ml; 100 mmol). The reaction medium is maintained under agitation for 1 hour at ambient temperature, then hydrolyzed at 0° C. by adding hydrochloric acid at 10%, agitated for 1 hour, and neutralized with sodium hydroxide. The resulting mixture is extracted with ethyl acetate. The combined extracts are washed with water and with a saturated solution of sodium chloride, then dried over magnesium sulphate and concentrated to produce 3.5 g of the desired product, in the form of a white solid (m.p.: 100–101° C.). hydrolyzed at 0° C. The resulting mixture is extracted with ethyl acetate The combined extracts are washed with water and with a saturated solution of sodium chloride dried over magnesium sulphate concentrated
来源 ID: ord-e6cc5972e0284db296af16c3ce022198反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2-aminobenzonitrile (4.25 g, 36 mmol) in anhydrous diethyl ether (40 ml) at 0° C. is treated under argon with benzylmagnesium chloride (2M in tetrahydrofuran; 50 ml; 100 mmol). The reaction medium is maintained under agitation for 1 hour at ambient temperature, then hydrolyzed at 0° C. by adding hydrochloric acid at 10%, agitated for 1 hour, and neutralized with soda. The resulting mixture is extracted with ethyl acetate. The combined extracts are washed with water and with a saturated solution of sodium chloride, then dried over magnesium sulphate and concentrated to produce 3.5 g of the desired product, in the form of a white solid (m.p.: 100–101° C.). hydrolyzed at 0° C. The resulting mixture is extracted with ethyl acetate The combined extracts are washed with water and with a saturated solution of sodium chloride dried over magnesium sulphate concentrated
来源 ID: ord-4a4a49a3ce5c4056b46634c5b240a433PubChem References
以下资料来自该化合物的公开数据库参考记录。
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