反応 #4167297
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-55c385b2d83f4590ad4e2701095f9b42表示可能な構造データがありません
C1=CC=C(C=C1)CC(=O)C2=CC=CC=C2N製品情報
1-(2-aminophenyl)-2-phenylethanone (CAS 835-38-1) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 577820
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
9 反応 · 9 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-55c385b2d83f4590ad4e2701095f9b42反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f37d5de2dacd40018b33ce7bfc019fca反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-55c385b2d83f4590ad4e2701095f9b42反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f37d5de2dacd40018b33ce7bfc019fca反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-4a4a49a3ce5c4056b46634c5b240a433反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-76ca4682e42a4d088ec5291911f05da8反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-76ca4682e42a4d088ec5291911f05da8反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-e6cc5972e0284db296af16c3ce022198反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-4a4a49a3ce5c4056b46634c5b240a433PubChem References
化合物の公開データベース記録に掲載された情報源です。
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