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Stannous chloride dihydrate → Methyl 3-aminocinnamate

HRID 226158
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HRID 226158 반응식
[CH3:1][O:2][C:3](=[O:15])[CH:4]=[CH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-])=O)[CH:7]=1.O.O.Cl[Sn]Cl>C(O)C>[CH3:1][O:2][C:3](=[O:15])[CH:4]=[CH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([NH2:12])[CH:7]=1
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참가 물질

4

반응물 2

HCID 61436Stannous chloride dihydrateHCID 1018253-(3-Nitrophenyl)acrylic acid methyl ester

생성물 1

HCID 54385173Methyl 3-aminocinnamate

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
80 °C

실험 절차

A mixture of 3-(3-nitro-phenyl)-acrylic acid methyl ester (22) (10.0 g, 48 mmol) and SnCl2.2H2O (54 g, 240 mmol) in anhydrous ethanol (200 ml) was heated at 80° C. for 1 hour. The reaction mixture was allowed to cool to room temperature, then the solvent was partially evaporated by vacuum rotary evaporator (up to ca. ½ volume). The residue was poured in ice water, neutralised (pH˜7) with saturated Na2CO3 and the resulting mixture was extracted with ethyl acetate. The organic extract was washed with saturated NaCl and dried (Na2SO4). The extract was filtrated through a small amount of silicagel and evaporated to give pure title compound in a form of white crystals (8.5 g, 99%). 1H NMR (CDCl3, HMDSO), δ: 3.69 (2H, br s); 3.79 (3H, s); 6.39 (1H, d, J=16.0 Hz); 6.61-7.03 (3H, m); 7.18 (1H, t, J=7.6 Hz); 7.62 (1H, d, J=16.0 Hz).

후처리

  1. temperatureto cool to room temperature
  2. customthe solvent was partially evaporated by vacuum rotary evaporator (up to ca. ½ volume)
  3. additionThe residue was poured in ice water
  4. extractionneutralised (pH˜7) with saturated Na2CO3 and the resulting mixture was extracted with ethyl acetate
  5. extractionThe organic extract
  6. washwas washed with saturated NaCl
  7. dry with materialdried (Na2SO4)
  8. filtrationThe extract was filtrated through a small amount of silicagel
  9. customevaporated

출처 및 근거

ORD 기록
ord-ca5b2a1f4aea4afe80408d3e06777ef1
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07557140B2

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