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Methyl iodide → HCID 178503083、化合物

HRID 1471854
ノート
印刷プレビュー

反応式

HRID 1471854 の反応式
[C:1]([C:4]1C=CC=[CH:6][CH:5]=1)(=O)[CH3:2].[C:10](=[S:12])=S.[H-].[Na+].IC.[NH2:17][NH2:18].[CH2:19]1[CH2:23]O[CH2:21][CH2:20]1>>[CH3:10][S:12][C:21]1[NH:18][N:17]=[C:19]([C:23]2[CH:6]=[CH:5][CH:4]=[CH:1][CH:2]=2)[CH:20]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 6

HCID 6328Methyl iodideHCID 6348Carbon DisulfideHCID 7410AcetophenoneHCID 8028TetrahydrofuranHCID 9321HydrazineHCID 24758Sodium hydride

生成物 1

HCID 178503083HCID 178503083、化合物

実験手順

To a solution of acetophenone (5.0 g, 41.6 mmol) and CS2 (3.17 g, 41.6 mmol) in THF (150 mL) was added sodium hydride (1.997 g, 83 mmol) at 0° C. After 30 min at 0° C., the reaction was warmed to room temperature and stirred for 1 h, then refluxed for 4 h. The reaction was cooled to room temperature, added iodomethane (16.23 g, 104 mmol), and refluxed for another 12 h. The reaction was cooled and extracted with ethyl acetate. The organic extracts were concentrated under reduced pressure. The residue was diluted with ethanol (200 mL), added hydrazine (1.334 g, 41.6 mmol), and refluxed for 4 h. After cooling, the mixture was concentrated under reduced pressure and extracted with ethyl acetate. The organic extracts were dried over MgSO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (6.02 g). LCMS m/z=191.37 [M+H]+; 1H NMR (400 MHz, DMSO-d6) δ ppm 2.31 (s, 3H), 6.21 (s, 1H), 7.38-7.56 (m, 5H), 12.2 (s, 1H).

後処理

  1. temperaturerefluxed for 4 h
  2. temperatureThe reaction was cooled to room temperature
  3. temperaturerefluxed for another 12 h
  4. temperatureThe reaction was cooled
  5. extractionextracted with ethyl acetate
  6. concentrationThe organic extracts were concentrated under reduced pressure
  7. additionThe residue was diluted with ethanol (200 mL)
  8. temperaturerefluxed for 4 h
  9. temperatureAfter cooling
  10. concentrationthe mixture was concentrated under reduced pressure
  11. extractionextracted with ethyl acetate
  12. dry with materialThe organic extracts were dried over MgSO4
  13. concentrationconcentrated under reduced pressure
  14. customThe residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-fd5815c9d858487d939490a379418faf
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09012478B2

反応ノート

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