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

Lithium Hydroxide → HCID 74943869, Verbindung

HRID 2427930
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2427930
[CH3:1][C:2]([CH3:8])([CH3:7])[C:3](=[N:5][OH:6])[CH3:4].[Li+].[OH-].[CH2:11]1[O:13][CH2:12]1>O>[OH:13][CH2:12][CH2:11][O:6][N:5]=[C:3]([C:2]([CH3:8])([CH3:7])[CH3:1])[CH3:4]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 3939Lithium HydroxideHCID 6354Ethylene OxideHCID 137609N-(3,3-Dimethylbutan-2-ylidene)hydroxylamine

Produkt 1

HCID 74943869HCID 74943869, VerbindungAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

400 ml of water, 92 g (0.8 mol) of 3,3-dimethylbutan-2-one oxime and 3.4 g of LiOH were initially charged, and 70 g (1.6 mol) of ethylene oxide were introduced such that the gas was taken up completely. Thereafter, the mixture was stirred at room temperature (RT) for 8-12 hours for the continued reaction. The upper phase was removed, admixed with ethyl acetate and washed with water. The organic phase was concentrated under reduced pressure at 100-200 mbar. Residue: 114-120 g of colorless oil, which corresponds to a yield of 90% yield; b.p. 106° C./35 mbar.

Aufarbeitung

  1. customfor the continued reaction
  2. customThe upper phase was removed
  3. washwashed with water
  4. concentrationThe organic phase was concentrated under reduced pressure at 100-200 mbar

Quellen und Nachweise

ORD-Eintrag
ord-01bef4b727d14d56b3db211d3f892815
Quelldatensatz
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07968747B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion