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

HRID 906601
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HRID 906601 반응식
[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]
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참가 물질

5

반응물 2

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

생성물 1

HCID 53424411Methyl 2-amino-4-ethyl-5-iodobenzoate수율 73%

시약·촉매·용매 2

HCID 159865Silver sulfate촉매HCID 702Ethanol용매

실험 절차

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

후처리

  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)

출처 및 근거

ORD 기록
ord-313fc481338a4cf48f81918726e9970b
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08012988B2

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