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Cyclohexane → 4,5-Dimethyl-2-[2-(methylsulfanyl)ethyl]-1,3-oxathiolane

HRID 462566
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 462566
[CH2:1]1[CH2:6]CCC[CH2:2]1.[SH:7][CH:8]([CH3:12])[CH:9]([OH:11])[CH3:10].CCC[CH:16]=[S:17]>O>[CH3:12][CH:8]1[CH:9]([CH3:10])[O:11][CH:2]([CH2:1][CH2:6][S:17][CH3:16])[S:7]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8078CyclohexaneHCID 620872-Mercapto-3-butanolHCID 12463483Butanthial

Produkt 1

HCID 203986674,5-Dimethyl-2-[2-(methylsulfanyl)ethyl]-1,3-oxathiolane

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Into a 100 ml reaction flask equipped with spin bar, reflux condenser, heating mantle, hot plate apparatus (with magnetic stirring apparatus) is placed 5 ml cyclohexane, 0.2 grams paratoluenesulfonic acid and 5.3 grams (0.05 moles) of 3-mercapto-2-butanol. Over a period of 30 minutes, 5.2 grams (0.05 moles) of 3-methylthiopropionaldehyde are added to the reaction mass. The reaction mass is then heated to reflux and water of reaction is continuously removed during the refluxing of the reaction mass. The reaction takes place over a period of 7 hours. At the end of the 7 hours the reaction mass is transferred to a separatory funnel and the reaction mass is washed with one 50 ml portion of saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate. The product is then filtered and distilled on a Microvigreux column yielding the following fractions:

Aufarbeitung

  1. customInto a 100 ml reaction flask
  2. customequipped with spin bar
  3. temperaturereflux condenser
  4. temperatureheating mantle
  5. temperatureThe reaction mass is then heated
  6. temperatureto reflux
  7. customis continuously removed during the
  8. temperaturerefluxing of the reaction mass
  9. customof 7 hours
  10. customAt the end of the 7 hours the reaction mass is transferred to a separatory funnel
  11. washthe reaction mass is washed with one 50 ml portion of saturated aqueous sodium chloride solution
  12. dry with materialdried over anhydrous sodium sulfate
  13. filtrationThe product is then filtered
  14. distillationdistilled on a Microvigreux column
  15. customyielding the following fractions

Quellen und Nachweise

ORD-Eintrag
ord-47f1e58a12d94fbf9d97db139d04339c
Quelldatensatz
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04515966

Notizen zur Reaktion

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