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4-Toluenesulfonyl chloride → 2-Tosylthiophene

HRID 2267332
ノート
印刷プレビュー

反応式

HRID 2267332 の反応式
[C:1]1([CH3:11])[CH:6]=[CH:5][C:4]([S:7](Cl)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[S:12]1[CH:16]=[CH:15][CH:14]=[CH:13]1>C(#N)C.[Cl-].[Zn+2].[Cl-]>[S:7]([C:13]1[S:12][CH:16]=[CH:15][CH:14]=1)([C:4]1[CH:5]=[CH:6][C:1]([CH3:11])=[CH:2][CH:3]=1)(=[O:9])=[O:8]
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 73974-Toluenesulfonyl chlorideHCID 8030Thiophene

生成物 1

HCID 2555212-Tosylthiophene収率 95.5%

試薬・触媒・溶媒 2

HCID 3007855Zincchloride触媒HCID 6342Acetonitrile溶媒

実験手順

A mixture of p-toluenesulfonyl chloride (3 g, 15.7 mmol) and zinc chloride (3 g, 21.3 mmol) in acetonitrile (30 mL) was heated to reflux and thiophene (2.4 g, 28.5 mmol) was added dropwise. After refluxing for 4 h the mixture was cooled to rt and filtered through Celite. The filtrate was concentrated in vacuo and then 100 mL of sodium hydroxide (2 N) was added. The mixture was extracted with ethyl acetate (3×60 mL) and the combined organic layers were washed with hydrochloric acid (10%, 50 mL) and brine (100 mL), dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated in vacuo and the product was purified by flash chromatography eluting with dichloromethane/hexane (2:3) to give the title compound (0.54 g, 15 mmol).

後処理

  1. temperaturewas heated
  2. temperatureto reflux
  3. temperatureAfter refluxing for 4 h the mixture
  4. filtrationfiltered through Celite
  5. concentrationThe filtrate was concentrated in vacuo
  6. addition100 mL of sodium hydroxide (2 N) was added
  7. extractionThe mixture was extracted with ethyl acetate (3×60 mL)
  8. washthe combined organic layers were washed with hydrochloric acid (10%, 50 mL) and brine (100 mL)
  9. dry with materialdried over anhydrous magnesium sulfate
  10. filtrationfiltered
  11. customThe solvent was evaporated in vacuo
  12. customthe product was purified by flash chromatography
  13. washeluting with dichloromethane/hexane (2:3)

出典と根拠

ORDレコード
ord-dcd43305a0ed45b6af4702663bdb4623
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07858785B2

反応ノート

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