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Iodine → Methyl 2-amino-4-ethyl-5-iodobenzoate

HRID 906601
ノート
印刷プレビュー

反応式

HRID 906601 の反応式
[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH3:11])=[CH:6][C:5]=1[NH2:12].[I:14]I>CCO.[O-]S([O-])(=O)=O.[Ag+].[Ag+]>[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[C:8]([I:14])[C:7]([CH2:10][CH3:11])=[CH:6][C:5]=1[NH2:12]
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 2

HCID 807IodineHCID 59164409Methyl 2-amino-4-ethylbenzoate

生成物 1

HCID 53424411Methyl 2-amino-4-ethyl-5-iodobenzoate収率 73%

試薬・触媒・溶媒 2

HCID 159865Silver sulfate触媒HCID 702Ethanol溶媒

実験手順

To a solution of 2-amino-4-ethyl-benzoic acid methyl ester (500 mg, 2.79 mmol) in EtOH (2 mL) were added Ag2SO4 (868.15 mg, 2.79 mmol) and I2 (708.1 mg, 2.79 mmol) and the resultant mixture was stirred at r.t. for 3 h. The reaction mixture was filtered and the solvent was removed in vacuo. The residue was dissolved in EtOAc and the organic phase was washed with 1M Na2S2O3 and sat. aq NaHCO3. The solvent was removed in vacuo and the orange oil was purified by flash chromatography (silica gel, hexanes→4:1 hexanes:EtOAc) to provide the title compound (620 mg, 73%) as an orange solid. ESI-MS: m/z 306.2 [M+H]+, rt 6.03 min

後処理

  1. filtrationThe reaction mixture was filtered
  2. customthe solvent was removed in vacuo
  3. dissolutionThe residue was dissolved in EtOAc
  4. washthe organic phase was washed with 1M Na2S2O3 and sat. aq NaHCO3
  5. customThe solvent was removed in vacuo
  6. customthe orange oil was purified by flash chromatography (silica gel, hexanes→4:1 hexanes:EtOAc)

出典と根拠

ORDレコード
ord-313fc481338a4cf48f81918726e9970b
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08012988B2

反応ノート

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