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Potassium Carbonate → 4-Methoxy-3-(3-morpholinopropoxy)benzonitrile

HRID 715683
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 715683
[N:1]1([CH2:7][CH2:8][CH2:9][OH:10])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.CS(Cl)(=O)=O.C(=O)([O-])[O-].[K+].[K+].O[C:23]1[CH:24]=[C:25]([CH:28]=[CH:29][C:30]=1[O:31][CH3:32])[C:26]#[N:27]>ClCCl>[CH3:32][O:31][C:30]1[CH:29]=[CH:28][C:25]([C:26]#[N:27])=[CH:24][C:23]=1[O:10][CH2:9][CH2:8][CH2:7][N:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 11430Potassium CarbonateHCID 31297Methanesulfonyl chlorideHCID 1995763-Morpholino-1-propanolHCID 49128223-Hydroxy-4-methoxybenzonitrile

Produkt 1

HCID 103560884-Methoxy-3-(3-morpholinopropoxy)benzonitrile

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344
Dichloromethane
Lösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

5 g 3-Morpholine-4-yl-propan-1-ol was dissolved in dichloromethane, cooled to 0° C., 3.25 mL methanesulfonylchloride was added and the mixture was stirred for 2 h at ambient temperature. Then 7 g potassium carbonate and 3-hydroxy-4-methoxybenzonitrile were added and the reaction was stirred at 45° C. for 3 h. The mixture was concentrated and 70 mL dimethylacetamide was added and stirred at 120° C. for 3 h. After this time, the mixture was diluted with dichloromethane and extracted with water, the organic phase was dried over magnesium sulfate and concentrated.

Aufarbeitung

  1. stirringthe reaction was stirred at 45° C. for 3 h
  2. concentrationThe mixture was concentrated
  3. addition70 mL dimethylacetamide was added
  4. stirringstirred at 120° C. for 3 h
  5. additionAfter this time, the mixture was diluted with dichloromethane
  6. extractionextracted with water
  7. dry with materialthe organic phase was dried over magnesium sulfate
  8. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-7af5c63f4222416bbf2ffc0f49886eaf
Quelldatensatz
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09187478B2

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