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

Diethyl Ether → HCID 58827413, Verbindung

HRID 2378141
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2378141
[C:1]1([CH3:22])[CH:6]=[C:5]([CH3:7])[CH:4]=[C:3]([CH3:8])[C:2]=1[N:9]=[CH:10][CH:11]=[N:12][C:13]1[C:18]([CH3:19])=[CH:17][C:16]([CH3:20])=[CH:15][C:14]=1[CH3:21].[CH2:23]([Li])[CH2:24][CH2:25][CH3:26].[CH3:28][CH2:29][CH2:30][CH2:31]CC.C(OCC)C>C1COCC1.O>[C:1]1([CH3:22])[CH:6]=[C:5]([CH3:7])[CH:4]=[C:3]([CH3:8])[C:2]=1[NH:9][CH:10]([CH:11]([NH:12][C:13]1[C:14]([CH3:21])=[CH:15][C:16]([CH3:20])=[CH:17][C:18]=1[CH3:19])[CH2:28][CH2:29][CH2:30][CH3:31])[CH2:23][CH2:24][CH2:25][CH3:26]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 3283Diethyl EtherHCID 8058HexaneHCID 3741651N,N'-1,2-Ethanediylidenebis(2,4,6-trimethylbenzenamine)HCID 178418339Butyllithium

Produkt 1

HCID 58827413HCID 58827413, VerbindungAusbeute 65 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962
Water
Lösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

In a 150 ml Schlenk vessel, N,N′-dimesitylethanediimine (2.92 g; 10 mmol) was dissolved in 30 ml of THF under nitrogen as protective gas and the solution was cooled to −78° C. 1.6 M Butyllithium in hexane (13.8 ml; 22 mmol) was then slowly added to the resulting suspension at −78 ° C. The reaction mixture was warmed to −10° C. over a period of one hour and was stirred at this temperature for a further hour. The solvent was then taken off and 15 ml of diethyl ether and 10 ml of water were then added on an ice bath. The aqueous layer was extracted with 2×5 ml of ether and the combined extracts were dried over powdered NaOH. Taking off the solvent left an orange oil. The crude product was chromatographed on a silica gel column (50 g) and eluted with petroleum ether/toluene (1:1). Taking off the solvent gave yellow crystals of dl-N,N′-dimesityldecane-5,6-diamine (2.67 g; 65%).

Aufarbeitung

  1. temperatureThe reaction mixture was warmed to −10° C. over a period of one hour
  2. extractionThe aqueous layer was extracted with 2×5 ml of ether
  3. customthe combined extracts were dried
  4. waitleft an orange oil
  5. customThe crude product was chromatographed on a silica gel column (50 g)
  6. washeluted with petroleum ether/toluene (1:1)

Quellen und Nachweise

ORD-Eintrag
ord-7b69dc1422c74450ae8ec797bd949ee3
Quelldatensatz
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07470750B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion