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Thiophenol → 2-((Phenylsulfanyl)methyl)oxirane

HRID 1901734
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1901734
[C:1]1([SH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:8]([CH:10]1[O:12][CH2:11]1)Br.[OH-].[Na+]>O1CCOCC1>[C:1]1([S:7][CH2:8][CH:10]2[CH2:11][O:12]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 7969ThiophenolHCID 14798Sodium HydroxideHCID 18430Epibromohydrin

Produkt 1

HCID 110949982-((Phenylsulfanyl)methyl)oxirane

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel2×

Versuchsvorschrift

A solution of 5.0 g of thiophenol in 30 ml of 1,4-dioxane was added dropwise at room temperature to a mixture of 6 ml of epibromohydrin, 5.45 g of sodium hydroxide and 30 ml of 1,4-dioxane, and then the mixture was stirred at room temperature for 36 hours. At the end of this time, insoluble solids were removed by filtration, the 1,4-dioxane was evaporated from the filtrate, water was added to the resulting residue, and the mixture was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The ethyl acetate was removed from the extract by evaporation under reduced pressure, and the resulting residue was purified by silica gel column chromatography, using a 1:10 by volume mixture of ethyl acetate and hexane as the eluent, to give 6.78 g of the title compound as a colorless oil having an Rf value of 0.60 (on silica gel thin layer chromatography, using a 1:10 by volume mixture of ethyl acetate and hexane as the developing solvent).

Aufarbeitung

  1. customAt the end of this time, insoluble solids were removed by filtration
  2. customthe 1,4-dioxane was evaporated from the filtrate, water
  3. additionwas added to the resulting residue
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe extract was washed with an aqueous solution of sodium chloride
  6. dry with materialdried over anhydrous sodium sulfate
  7. customThe ethyl acetate was removed from the
  8. extractionextract by evaporation under reduced pressure
  9. customthe resulting residue was purified by silica gel column chromatography
  10. additionby volume mixture of ethyl acetate and hexane as the eluent

Quellen und Nachweise

ORD-Eintrag
ord-aa3a9be7bde745e89d14988705fc67d5
Quelldatensatz
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05578620

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