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Ethanol → 1-(4-Amino-2-chlorophenoxy)-2-bromoethane

HRID 1106870
ノート
印刷プレビュー

反応式

HRID 1106870 の反応式
[Cl:1][C:2]1[CH:11]=[C:10]([N+:12]([O-])=O)[CH:9]=[CH:8][C:3]=1[O:4][CH2:5][CH2:6][Br:7].C(O)C.[O-]S(S([O-])=O)=O.[Na+].[Na+]>O>[NH2:12][C:10]1[CH:9]=[CH:8][C:3]([O:4][CH2:5][CH2:6][Br:7])=[C:2]([Cl:1])[CH:11]=1
参加物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 702EthanolHCID 24489Sodium DithioniteHCID 3099731-(2-bromoethoxy)-2-chloro-4-nitrobenzene

生成物 1

HCID 187898501-(4-Amino-2-chlorophenoxy)-2-bromoethane収率 23.5%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To 11 g (0.040 mol) of the 1-(2-chloro-4-nitrophenoxy)-2-bromoethane produced in Example 5-(1), ethanol (170 ml) was added and dissolved therein; to the resulting solution, Na2S2O4 (27.6 g, 0.158 mol) as dissolved in water (50 ml) was added dropwise, followed by stirring at room temperature for 20 min. The solvent was evaporated and the residue was diluted with an aqueous solution of sodium bicarbonate and two extractions were conducted with ethyl acetate. The organic extracts were dried with sodium sulfate and the solvent was evaporated, with the residue being purified by being subjected to column chromatography on silica gel using, as an eluent, n-hexane containing ethyl acetate (25%) to yield the end compound 1-(4-amino-2-chlorophenoxy)-2-bromoethane (2.35 g) as a pale yellow solid mass.

後処理

  1. dissolutiondissolved
  2. additionwas added dropwise
  3. customThe solvent was evaporated
  4. additionthe residue was diluted with an aqueous solution of sodium bicarbonate and two extractions
  5. dry with materialThe organic extracts were dried with sodium sulfate
  6. customthe solvent was evaporated, with the residue
  7. custombeing purified
  8. additionn-hexane containing ethyl acetate (25%)

出典と根拠

ORDレコード
ord-a18f57c282a24535b0600d15ce670401
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

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