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llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
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Water → 6-Chloroundecane

HRID 23801
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 23801
CS(O[CH:6]([CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])(=O)=O.[Cl-:17].[Li+].O>CN(C)C=O>[Cl:17][CH:6]([CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 433294Lithium ChlorideHCID 225905206-Methanesulfonyloxyundecane

Produkt 1

HCID 99206036-ChloroundecaneAusbeute 97,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
15 °C

Versuchsvorschrift

Thirty grams (0.12 mol) of 6-methanesulfonyloxyundecane was dissolved in 150 mL of N,N-dimethylformamide and 15.3 g (0.36 mol) of anhydrous lithium chloride was added to the solution under cooling with ice. The mixture was warmed to 50˜55° C. and stirred for 3 hours. Thereafter, the mixture was cooled to 15° C. and 300 mL of cold water was added. The reaction mixture was extracted three times with 150 mL of hexane and the organic layer was sequentially washed with 150 mL of water and 150 mL of a saturated aqueous solution of sodium chloride and thereafter dried over 6 g of anhydrous magnesium sulfate. After filtering off the anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure to give 22.2 g (97.1% in yield) of 6-chloroundecane.

Aufarbeitung

  1. temperatureunder cooling with ice
  2. temperatureThe mixture was warmed to 50˜55° C.
  3. extractionThe reaction mixture was extracted three times with 150 mL of hexane
  4. washthe organic layer was sequentially washed with 150 mL of water and 150 mL of a saturated aqueous solution of sodium chloride
  5. dry with materialdried over 6 g of anhydrous magnesium sulfate
  6. filtrationAfter filtering off the anhydrous magnesium sulfate
  7. distillationthe solvent was distilled off under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-552f94c5b02243eb9ca1115a3c9d097d
Quelldatensatz
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06852867B2

Notizen zur Reaktion

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