ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

1,1-Dibromoethane → 1-(2-bromoethoxy)-2-chloro-4-nitrobenzene

HRID 1106864
ノート
印刷プレビュー

反応式

HRID 1106864 の反応式
[Br:1][CH:2](Br)[CH3:3].[Cl:5][C:6]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[CH:9]=[CH:8][C:7]=1[OH:15]>C(=O)([O-])[O-].[K+].[K+].O>[Cl:5][C:6]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[CH:9]=[CH:8][C:7]=1[O:15][CH2:3][CH2:2][Br:1]
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 2

HCID 112011,1-DibromoethaneHCID 12074Nitrofungin

生成物 1

HCID 3099731-(2-bromoethoxy)-2-chloro-4-nitrobenzene収率 86.6%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 11430Potassium Carbonate溶媒

反応条件

温度
85 °C

実験手順

Dibromoethane (14.9 ml, 0.1728 mol) and 2-chloro-4-nitrophenol (10 g, 0.0576 mol) were dissolved in dimethylfomamide (250 ml) and potassium carbonate (9.55 g) was added to the resulting solution, followed by stirring at 85° C. for 30 min. Thereafter, the reaction solution was diluted with water and subjected to three extractions with ethyl acetate. The organic extracts were combined, dried with magnesium and the solvent was evaporated; thereafter, the residue was purified by being subjected to column chromatography using a 1:1 solvent system of n-hexane and ethyl acetate as an eluent and the fractions containing the end product were collected and subjected to evaporation to yield the end compound 1-(2-chloro-4-nitrophenoxy)-2-bromoethane (14.0 g) as a yellow solid mass.

後処理

  1. additionwas added to the resulting solution
  2. extractionsubjected to three extractions with ethyl acetate
  3. dry with materialdried with magnesium
  4. customthe solvent was evaporated
  5. customthereafter, the residue was purified
  6. additionthe fractions containing the end product
  7. customwere collected
  8. customsubjected to evaporation

出典と根拠

ORDレコード
ord-e0c3fcc476fb47c5a5986c65e1824f45
出典データセット
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06057358

反応ノート

読み込み中…

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