Triphenylphosphine → 4-[2-(4-Bromo-3-fluorophenoxy)ethyl]morpholine

HRID 2427456Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2427456
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[F:9].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[O:29]1[CH2:34][CH2:33][N:32]([CH2:35][CH2:36]O)[CH2:31][CH2:30]1.N(C(OC(C)C)=O)=NC(OC(C)C)=O>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:36][CH2:35][N:32]2[CH2:33][CH2:34][O:29][CH2:30][CH2:31]2)=[CH:4][C:3]=1[F:9]

Komponenten

6

Edukt 4

HCID 11776TriphenylphosphineHCID 611632-MorpholinoethanolHCID 75555Diisopropyl diazene-1,2-dicarboxylateHCID 27791534-Bromo-3-fluorophenol

Produkt 1

HCID 590007294-[2-(4-Bromo-3-fluorophenoxy)ethyl]morpholineAusbeute 33 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A flask was charged with 4-bromo-3-fluorophenol (4.999 g, 26.2 mmol) and triphenylphosphine (10.298 g, 39.3 mmol). Methylene chloride (120 mL) was added followed by 2-morpholinoethanol (4 mL, 33.0 mmol) and the solution was stirred on an ice water bath to cool. After 5 minutes, diisopropyl azodicarboxylate (7.6 ml, 39.1 mmol) was added over 6 to 8 minutes. The reaction was left stirring on the cold bath to slowly warm to room temperature overnight. The reaction was concentrated and the residue purified by flash chromatography (25% to 100% EtOAc in hexanes) to provide the product as a colorless oil (2.621 g, 33%).

Aufarbeitung

  1. temperatureto cool
  2. waitThe reaction was left
  3. stirringstirring on the cold bath
  4. concentrationThe reaction was concentrated
  5. customthe residue purified by flash chromatography (25% to 100% EtOAc in hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-6c6846fff8fb4b318007952b9dfff9af
Quelldatensatz
uspto-grants-2011_06
Patentnummer
US07968574B2

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