p-Toluenesulfonic acid → 2-(4,5-Dimethyl-1,3-dithiolan-2-yl)furan

HRID 462577

反応式

HRID 462577 の反応式
C1(C)C=CC(S(O)(=O)=O)=CC=1.[CH3:12][CH:13]([SH:17])[CH:14]([SH:16])[CH3:15].[O:18]1[CH:22]=[CH:21][CH:20]=[C:19]1[CH:23]=O>C1CCCCC1>[O:18]1[CH:22]=[CH:21][CH:20]=[C:19]1[CH:23]1[S:17][CH:13]([CH3:12])[CH:14]([CH3:15])[S:16]1

参加物

5

実験手順

Into a 100 ml reaction flask equipped with magnetic stirring bar, thermometer and reflux condenser and hot plate with magnetic stirring apparatus is placed 0.5 grams para-toluenesulfonic acid, 5 ml cyclohexane and 6.1 grams (0.05 moles) of 2,3-butanedithiol. Over a period of 35 minutes, 4.8 grams (0.05 moles) of 2-furaldehyde is added to the reaction mass with stirring. The reaction mass is then heated to reflux and refluxed for a period of 7.5 hours with stirring while removing water of reaction. After the refluxing period, the reaction mass is cooled to room temperature and transferred to a separatory funnel. The reaction mass is then washed with one 50 ml portion of saturated sodium chloride solution and dried over anhydrous sodium sulfate and filtered. The resulting filtrate is distilled using a Microvigreux column yielding the following fractions:

後処理

  1. customInto a 100 ml reaction flask
  2. customequipped with magnetic stirring bar
  3. temperaturethermometer and reflux condenser
  4. temperatureThe reaction mass is then heated
  5. temperatureto reflux
  6. temperaturerefluxed for a period of 7.5 hours
  7. stirringwith stirring
  8. customwhile removing
  9. customwater of reaction
  10. customtransferred to a separatory funnel
  11. washThe reaction mass is then washed with one 50 ml portion of saturated sodium chloride solution
  12. dry with materialdried over anhydrous sodium sulfate
  13. filtrationfiltered
  14. distillationThe resulting filtrate is distilled
  15. customyielding the following fractions

出典と根拠

ORDレコード
ord-d4c2f66f3b2c455ab6ae07b7c9240dce
出典データセット
uspto-grants-1985_05
特許番号
US04515968

関連ノート

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