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Ammonium Chloride → HCID 22033543、化合物

HRID 325028
ノート
印刷プレビュー

反応式

HRID 325028 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([O:10][CH2:11][CH2:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]#[N:20])=[CH:15][CH:14]=2)[CH:5]=1)([O-])=O.[NH4+].[Cl-]>CCO.O.[Fe]>[NH2:1][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([O:10][CH2:11][CH2:12][C:13]2[CH:14]=[CH:15][C:16]([C:19]#[N:20])=[CH:17][CH:18]=2)[CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 25517Ammonium ChlorideHCID 22033514Nitro-3-[2-(4-cyanophenyl)ethoxy]benzene

生成物 1

HCID 22033543HCID 22033543、化合物収率 85%

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

Nitro-3-[2-(4-cyanophenyl)ethoxy]benzene (3.0 g; 11.2 mmol; from step (i) above) and NH4Cl (2.9 g; 55 mmol) were dissolved in a mixture of EtOH (40 mL) and H2O (10 mL) and heated to reflux. Iron powder (3.0 g; 55 mmol) was added and heating was continued for 1 hour. The mixture was filtered, concentrated in vacuo and partitioned between water and CH2Cl2. After separation, the aqueous phase was extracted with CH2Cl2. The combined organic phases were dried (MgSO4) and the solvent was evaporated. Purification by flash chromatography (SiO2; toluene:EtOAc (9:1)) afforded 2.26 g (85%) of the sub-title compound.

後処理

  1. temperatureheated to reflux
  2. temperatureheating
  3. filtrationThe mixture was filtered
  4. concentrationconcentrated in vacuo
  5. custompartitioned between water and CH2Cl2
  6. customAfter separation
  7. extractionthe aqueous phase was extracted with CH2Cl2
  8. dry with materialThe combined organic phases were dried (MgSO4)
  9. customthe solvent was evaporated
  10. customPurification by flash chromatography (SiO2; toluene:EtOAc (9:1))

出典と根拠

ORDレコード
ord-8ef99bd1e03243c586593e9f31e39f13
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06221898B1

反応ノート

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