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Ammonium Chloride → 3-Iodo-4-methoxyaniline

HRID 1403210
ノート
印刷プレビュー

反応式

HRID 1403210 の反応式
[I:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[CH:5]=[CH:4][C:3]=1[O:11][CH3:12].[NH4+].[Cl-]>CO.O.[Fe]>[I:1][C:2]1[CH:7]=[C:6]([CH:5]=[CH:4][C:3]=1[O:11][CH3:12])[NH2:8]
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 948062-Iodo-1-methoxy-4-nitrobenzene

生成物 1

HCID 220545963-Iodo-4-methoxyaniline収率 92.3%

試薬・触媒・溶媒 3

HCID 23925Iron触媒HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

To 2-iodo-1-methoxy-4-nitrobenzene (485 mg, 1.74 mmol) suspended in methanol (6 mL) a solution of NH4Cl (465 mg, 8.69 mmol) in water (4.9 mL) and powdered Fe (290 mg, 5.192 mmol) were added and the mixture was heated to reflux for 3 h. The precipitate formed was filtered off and the filtrate was evaporated until the methanol was eliminated. After diluting with water and alkalinization with sodium carbonate the mixture was extracted with EtOAc (4×20 mL). The combined organic extracts were washed with brine (3×10 mL), water (10 mL), dried over sodium sulfate and the solvent was removed under vacuum. The crude dark oil was purified by flash chromatography on silica gel (hexane/EtOAc 1/1) to afford 400 mg of solid that was crystallized from n-pentane and diethyl ether to yield the title compound (363 mg, 83%).

後処理

  1. additionwere added
  2. temperaturethe mixture was heated
  3. temperatureto reflux for 3 h
  4. customThe precipitate formed
  5. filtrationwas filtered off
  6. customthe filtrate was evaporated until the methanol
  7. additionAfter diluting with water and alkalinization with sodium carbonate the mixture
  8. extractionwas extracted with EtOAc (4×20 mL)
  9. washThe combined organic extracts were washed with brine (3×10 mL), water (10 mL)
  10. dry with materialdried over sodium sulfate
  11. customthe solvent was removed under vacuum
  12. customThe crude dark oil was purified by flash chromatography on silica gel (hexane/EtOAc 1/1)

出典と根拠

ORDレコード
ord-6acd3cc46ddd433fb5a8d77c07c705a4
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08912200B2

反応ノート

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