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Benzyl mercaptan → 4-(Benzylsulfanyl)-1,3-thiazole

HRID 2165993
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2165993
[CH2:1]([SH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[O-].[Na+].Cl[C:13]1[N:14]=[CH:15][S:16][CH:17]=1>C(O)C>[C:2]1([CH2:1][S:8][C:13]2[N:14]=[CH:15][S:16][CH:17]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 7509Benzyl mercaptanHCID 10942334Sodium MethoxideHCID 135173944-Chloro-1,3-thiazole

Produkt 1

HCID 150771204-(Benzylsulfanyl)-1,3-thiazoleAusbeute 37,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel2×

Versuchsvorschrift

Benzylmercaptan (24.8 g) was added slowly to a solution of 10.8 g of sodium methoxide in 100 ml ethanol. After 10 minutes, the reaction mixture was heated to 65° and a solution of 23.8 g of 4-chlorothiazole [prepared by the method of P. Reynaud et al., Bull. Soc. Chim. France, 1735 (1962)] in 25 ml ethanol was added dropwise. When addition was complete, the reaction mixture was refluxed 36 hours. The reaction mixture was cooled, and the bulk of the solvent evaporated. Cold water (300 ml) was added to the residue, and the aqueous mixture was extracted with 200 ml ether followed by 200 ml methylene chloride. The combined organic solution was washed with brine, dried over magnesium sulfate, filtered and the solvent evaporated. Distillation of the resulting yellow oil gave 15.6 g of 4-(phenylmethylthio)thiazole, bp 122-134 (0.6 mm).

Aufarbeitung

  1. temperaturethe reaction mixture was heated to 65°
  2. additionWhen addition
  3. temperaturethe reaction mixture was refluxed 36 hours
  4. temperatureThe reaction mixture was cooled
  5. customthe bulk of the solvent evaporated
  6. additionCold water (300 ml) was added to the residue
  7. extractionthe aqueous mixture was extracted with 200 ml ether
  8. washThe combined organic solution was washed with brine
  9. dry with materialdried over magnesium sulfate
  10. filtrationfiltered
  11. customthe solvent evaporated
  12. distillationDistillation of the resulting yellow oil

Quellen und Nachweise

ORD-Eintrag
ord-79133d08ab234ddbaf2a479eadc656fc
Quelldatensatz
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04943312

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