StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

2,6-Dimethylthiophenol → 2-[(2,6-Dimethylphenyl)sulfanyl]ethan-1-ol

HRID 1389771
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1389771
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[SH:9].Cl[CH:11]([OH:13])[CH3:12]>[OH-].[Na+].O>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[S:9][CH2:12][CH2:11][OH:13]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 610452,6-DimethylthiophenolHCID 126390351-Chloroethan-1-ol

Produkt 1

HCID 27586362-[(2,6-Dimethylphenyl)sulfanyl]ethan-1-olAusbeute 95 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 14798Sodium HydroxideLösungsmittel

Versuchsvorschrift

35 g. 2,6-dimethyl thiophenol are dissolved in a solution of 15.6 g sodium hydroxide in 210 ml water, under stirring and inert atmospher. After complete dissolution 34 g chloro ethanol are added portionwise thereto and the milky suspension is thereafter heated to reflux for one hour. The mixture reverts to room temperature and is extracted three times with ester to isolate the thus formed oily product. The ethereous solutions are washed with water, dried on sodium sulphate, filtered and evaporated off. 2-(2,6-dimethyl phenylthio) 1-hydroxy ethane is obtained with a yield of 95%. It is further used for the next step without any purification

Aufarbeitung

  1. additionare added portionwise
  2. temperaturethe milky suspension is thereafter heated
  3. temperatureto reflux for one hour
  4. customreverts to room temperature
  5. extractionis extracted three times with ester
  6. customto isolate the thus formed oily product
  7. washThe ethereous solutions are washed with water
  8. customdried on sodium sulphate
  9. filtrationfiltered
  10. customevaporated off

Quellen und Nachweise

ORD-Eintrag
ord-059ad6b88140418dbc6aec51b76a43c2
Quelldatensatz
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04246267

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion