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Methanol → 1-Methoxy-2-dodecanol

HRID 720228
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 720228
[CH3:1][OH:2].[O:3]1[CH:5]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])[CH2:4]1>>[CH3:1][O:2][CH2:4][CH:5]([OH:3])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 887MethanolHCID 178581,2-Epoxydodecane

Produkt 1

HCID 137094341-Methoxy-2-dodecanol

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

The same reactor that was used in Production Example 5 was charged with 64 g (2 mol) of methanol and 2 g of boron trifluoride diethyl ether complex and then the mixture was raised to 60° C. Then, 184.3 g (1 mol) of 1,2-epoxydodecane was added dropwise to the mixture over one hour and the resulting mixture was kept as it was for 3 hours. The reaction was terminated just after confirming that 1,2-epoxydodecane left unreacted was less than 1% by gas chromatography and then the reaction mixture was cooled. Thereafter, methanol was removed in the same manner as in Production Example 5 to obtain 2-hydroxydodecyl methyl ether.

Aufarbeitung

  1. custom
The reaction was terminated just
  • waitleft unreacted
  • temperaturethe reaction mixture was cooled
  • customThereafter, methanol was removed in the same manner as in Production Example 5
  • Quellen und Nachweise

    ORD-Eintrag
    ord-db80ebc7b88445a794e1d3f12f9b1ff2
    Quelldatensatz
    uspto-grants-2006_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US07135443B2

    Notizen zur Reaktion

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