Triphenylphosphine → N-[3-(1-Methyl-piperidin-4-yloxy)-phenyl]-acetamide

HRID 44641

Reaktionsgleichung

Reaktionsgleichung von HRID 44641
[OH:1][C:2]1[CH:3]=[C:4]([NH:8][C:9](=[O:11])[CH3:10])[CH:5]=[CH:6][CH:7]=1.O[CH:13]1[CH2:18][CH2:17][N:16]([CH3:19])[CH2:15][CH2:14]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>O1CCCC1>[CH3:19][N:16]1[CH2:17][CH2:18][CH:13]([O:1][C:2]2[CH:3]=[C:4]([NH:8][C:9](=[O:11])[CH3:10])[CH:5]=[CH:6][CH:7]=2)[CH2:14][CH2:15]1

Komponenten

5

Edukt 3

HCID 11776Triphenylphosphine2×HCID 121243-HydroxyacetanilideHCID 660484-Piperidinol, 1-methyl-

Produkt 1

HCID 57444159N-[3-(1-Methyl-piperidin-4-yloxy)-phenyl]-acetamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

A suspension of N-(3-Hydroxy-phenyl)-acetamide (30.2 g) in anhydrous tetrahydrofuran (600 mL) was treated with 4-hydroxy-N-methylpiperidine (30.54 mL) and triphenylphosphine (68.18 g); a solution of diethylazadicarboxylate in anhydrous tetrahydrofuran (THF) (40.94 mL in 60 mL of THF) was added dropwise and the mixture was stirred at room temperature for 2 hours and then heated to 50° C. overnight. Further amounts of triphenylphosphine (28.00 g) and diethylazadicarboxylate (14 mL) were added and the heating was continued for additional 24 hours.

Aufarbeitung

  1. temperatureheated to 50° C. overnight
  2. additionwere added
  3. waitthe heating was continued for additional 24 hours

Quellen und Nachweise

ORD-Eintrag
ord-c4473f8be0684334b827e5bd7897e708
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08541429B2

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