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Ethyl Acetate → HCID 178510661、化合物

HRID 1769286
ノート
印刷プレビュー

反応式

HRID 1769286 の反応式
[C:1]([C:3]1[NH:7][C:6]([C:8]2[C:13]([Cl:14])=[CH:12][C:11]([C:15]([F:18])([F:17])[F:16])=[CH:10][C:9]=2[Cl:19])=[N:5][CH:4]=1)#[N:2].[Br:20]Br.C(OCC)(=O)C>ClC(Cl)C(Cl)Cl>[Br:20][C:4]1[N:5]=[C:6]([C:8]2[C:13]([Cl:14])=[CH:12][C:11]([C:15]([F:17])([F:16])[F:18])=[CH:10][C:9]=2[Cl:19])[NH:7][C:3]=1[C:1]#[N:2]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8857Ethyl AcetateHCID 24408BromineHCID 189476905-Cyano-2-(2,6-dichloro-4-trifluoromethylphenyl)imidazole

生成物 1

HCID 178510661HCID 178510661、化合物収率 169.2%

試薬・触媒・溶媒 1

HCID 65911,1,2,2-Tetrachloroethane溶媒

反応条件

温度
90 °C

実験手順

A mixture of 5-cyano-2-(2,6-dichloro-4-trifluoromethylphenyl)imidazole (1.0 g, 0.0033 mol) and bromine (1.9 g, 0.64 ml, 0.13 mol) in 1,1,2,2-tetrachloroethane (20 ml) was stirred and heated at 90° C. for 7 hours. Ethyl acetate (50 ml) was added and the solution was washed with water (50 ml), aqueous sodium metabisulphite solution (50 ml). water (50 ml), dried over anhydrous sodium sulphate and evaporated to dryness. The solid residue was purified by chromatography on silica gel elucing with a mixture of ethyl acetate and petroleum ether (b.p. 60°-80° C.)(3:10) to give 4-bromo-5-cyano-2-(2,6-dichloro-4-trifluoromethylphenyl)imidazole (2.15 g) as a white solid m.p. 270.5°-272° C.

後処理

  1. washthe solution was washed with water (50 ml), aqueous sodium metabisulphite solution (50 ml)
  2. dry with materialwater (50 ml), dried over anhydrous sodium sulphate
  3. customevaporated to dryness
  4. customThe solid residue was purified by chromatography on silica gel elucing with a mixture of ethyl acetate and petroleum ether (b.p. 60°-80° C.)(3:10)

出典と根拠

ORDレコード
ord-f870be53a61e4e6b9d8d27c3157d416c
出典データセット
uspto-grants-1995_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05380865

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート