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Hydrochloric Acid → HCID 16079271、化合物

HRID 722297
ノート
印刷プレビュー

反応式

HRID 722297 の反応式
CN(C)CCN(C)C.[Li]CCCC.[Cl:14][C:15]1[CH:20]=[CH:19][C:18]([SH:21])=[CH:17][CH:16]=1.CN([CH:25]=[O:26])C.Cl>C1CCCCC1>[Cl:14][C:15]1[CH:20]=[C:19]([CH:25]=[O:26])[C:18]([SH:21])=[CH:17][CH:16]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 6228DimethylformamideHCID 7815p-ChlorothiophenolHCID 8037N,N,N',N'-TetramethylethylenediamineHCID 178418339Butyllithium

生成物 1

HCID 16079271HCID 16079271、化合物収率 14.4%

試薬・触媒・溶媒 1

HCID 8078
Cyclohexane
溶媒

反応条件

温度
0 °C

実験手順

Tetramethylethylenediamine (TMEDA) (10.44 mL, 8.035 g, 69.15 mmol) was added via syringe to n-BuLi (43.22 mL of 1.6 M in hexanes, 69.15 mmol) and the solution was chilled to 0° C. A solution of 4-chlorothiophenol (5.00 g, 34.57 mmol) in cyclohexane (25 mL) was added with stirring over 1 hour. The resulting tan slurry was stirred overnight at room temperature, chilled to 0° C., and DMF (2.94 mL, 2.78 g, 38.03 mmol) was added via syringe over 2 minutes. The resulting gummy slurry was stirred at room temperature for 30 hours and became a powdery suspension. A mixture of 2 N HCl and ice was added to the reaction mixture until the pH became acidic (pH=1). During this addition, the mixture warmed and became first red and then pale yellow. This mixture was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo yielding a clear red-brown oil. This oil was triturated with hexanes yielding a red-brown semisolid. This semisolid was purified by plug flash chromatography over silica gel, eluting with 1:1, hexanes:dichloromethane to afford 5-chloro-thiosalicylaldehyde (0.858 g, 14%) as an intensely yellow solid suitable for use without further purification.

後処理

  1. stirringThe resulting tan slurry was stirred overnight at room temperature
  2. temperaturechilled to 0° C.
  3. stirringThe resulting gummy slurry was stirred at room temperature for 30 hours
  4. additionwas added to the reaction mixture until the pH
  5. additionDuring this addition
  6. temperaturethe mixture warmed
  7. extractionThis mixture was extracted with ethyl acetate
  8. washThe combined organic layers were washed with brine
  9. dry with materialdried over MgSO4
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo
  12. customyielding a clear red-brown oil
  13. customThis oil was triturated with hexanes yielding a red-brown semisolid
  14. customThis semisolid was purified by plug flash chromatography over silica gel
  15. washeluting with 1:1, hexanes

出典と根拠

ORDレコード
ord-f2183ab2bdfd480a963878bd7bd66463
出典データセット
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07138411B2

反応ノート

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