反応 #4163609
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-43a8b6fc6d2d424ab73d1cfd66c92311表示可能な構造データがありません
CC(=O)NC1=CC(=CC=C1)Br製品情報
N-(3-bromophenyl)acetamide (CAS 621-38-5) 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 12123
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
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-43a8b6fc6d2d424ab73d1cfd66c92311反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-816f3f6643bf4b4a8fe6587afc453a44反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-a31349d623694a49aa181b27b2b9c90f反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c1e95ec78bfa4b06904dc3fafd66fc60反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9dd06a3aeed64b4d8ba2ea4fe7dbab1b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-110661fada1a40b69ff93267927e0650反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-43a8b6fc6d2d424ab73d1cfd66c92311反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-816f3f6643bf4b4a8fe6587afc453a44反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-816f3f6643bf4b4a8fe6587afc453a44反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: In a manner similar to that of Example (27b), by reaction of 820 mg (20.5 mmol, 1.1 eq) of 60% sodium hydride, 4.0 g (18.7 mmol, 1 eq) of N-(3-bromophenyl)acetamide (prepared in Example 27a) and 2.20 mL (22.4 mmol, 1.2 eq) of 1-iodopropane in 15 ml of tetrahydrofuran in the presence of 1.5 ml of dimethylformamide, N-(3-bromophenyl)-N-propylacetamide is obtained in oil form and is used in the following reaction without further purification.
ソース ID: ord-b8c72420ab1243119e5a952cb08513ba反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: In a manner similar to that of Example (27b), by reaction of 820 mg (20.5 mmol, 1.1 eq) of 60% sodium hydride, 4.0 g (18.7 mmol, 1 eq) of N-(3-bromophenyl)acetamide (prepared in Example 27a) and 2.20 mL (22.4 mmol, 1.2 eq) of 1-iodopropane in 15 ml of tetrahydrofuran in the presence of 1.5 ml of dimethylformamide, N-(3-bromophenyl)-N-propylacetamide is obtained in oil form and is used in the following reaction without further purification.
ソース ID: ord-b8c72420ab1243119e5a952cb08513ba反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 820 mg (20.5 mmol, 1.1 eq) of 60% sodium hydride are added to a solution of 4.0 g (18.7 mmol, 1 eq) of N-(3-bromophenyl)acetamide and 1.80 mL (22.4 mmol, 1.2 eq) of ethyl iodide in 15 ml of tetrahydrofuran in the presence of 1.5 ml of dimethylformamide. The reaction medium is stirred at room temperature for 12 hours and then hydrolyzed with water and extracted with ethyl acetate. The organic phases are combined, washed with sodium chloride solution and dried over sodium sulfate. The solvents are evaporated off and the N-(3-bromophenyl)-N-ethylacetamide obtained in oil form is used in the following reaction without further purification. hydrolyzed with water and extracted with ethyl acetate washed with sodium chloride solution dried over sodium sulfate The solvents are evaporated off
ソース ID: ord-0f32b78ee59147788d54de37ff1276ddPubChem 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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