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Thionyl Chloride → 1-Chloro-2-methyl-6-phenoxy-hexane

HRID 2083106
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2083106
S(Cl)([Cl:3])=O.O[CH2:6][CH:7]([CH3:19])[CH2:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(Cl)(Cl)Cl.CN(C=O)C>[Cl:3][CH2:6][CH:7]([CH3:19])[CH2:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 24386Thionyl ChlorideHCID 203221341-Hydroxy-2-methyl-6-phenoxyhexane

Produkt 1

HCID 203221511-Chloro-2-methyl-6-phenoxy-hexane

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6212ChloroformLösungsmittel2×HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

A solution of 60 g of thionyl chloride in 50 ml of CHCl3 was added dropwise to 100 g of 1-Hydroxy-2-methyl-6-phenoxyhexane in 200 ml of CHCl3 and 0.5 ml of DMF. The solution was refluxed until the development of the gas was finished and then poured onto ice. The aqueous phase was extracted twice with CHCl3 and the combined organic phases were washed with water and finally with a saturated NaHCO3 -solution, dried with MgSO4, evaporated and the residue was distilled off. Boiling point0.5 : 117° - 120° C.

Aufarbeitung

  1. temperatureThe solution was refluxed until the development of the gas
  2. additionpoured onto ice
  3. extractionThe aqueous phase was extracted twice with CHCl3
  4. washthe combined organic phases were washed with water and finally with a saturated NaHCO3 -solution
  5. dry with materialdried with MgSO4
  6. customevaporated
  7. distillationthe residue was distilled off
  8. custom117° - 120° C.

Quellen und Nachweise

ORD-Eintrag
ord-8f7b55bb3ecb4d3ba29fd66b34a5ecf5
Quelldatensatz
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04083990

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