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Water → 2-((4-Bromobenzyl)oxy)pyridine

HRID 557263
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 557263
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][OH:7])=[CH:4][CH:3]=1.CC(C)([O-])C.[K+].F[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=1.O>CN(C)C=O.C(OCC)(=O)C>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][O:7][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][N:18]=2)=[CH:4][CH:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 962WaterHCID 97462-FluoropyridineHCID 701194-Bromobenzyl alcoholHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 247991602-((4-Bromobenzyl)oxy)pyridineAusbeute 99 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228
Dimethylformamide
Lösungsmittel
HCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
54 °C

Versuchsvorschrift

To a solution of 4-bromobenzyl alcohol (25 g, 130 mmol) in N,N-dimethyl formamide (125 mL) was added potassium tert-butoxide (15.8 g, 141 mmol) at room temperature, which was stirred at 54° C. for 10 minutes. To this reaction solution was added 2-fluoropyridine (15 mL, 154 mmol) at from 40° C to 58° C, which was stirred further at 65° C for 30 minutes. The reaction solution was allowed to room temperature, and water and ethyl acetate were added to carry out liquid separation. The aqueous layer was extracted further with ethyl acetate (twice). The ethyl acetate layers were combined, washed with water (three times) and sodium chloride water (once), dried over anhydrous magnesium sulfate and then filtered. The filtrate thereof was concentrated under a reduced pressure. To the residue was added diethyl ether, and concentrated under a reduced pressure to obtain the title compound (34 g) as a crude product.

Aufarbeitung

  1. stirringwas stirred further at 65° C for 30 minutes
  2. customwas allowed to room temperature
  3. customliquid separation
  4. extractionThe aqueous layer was extracted further with ethyl acetate (twice)
  5. washwashed with water (three times) and sodium chloride water (once),
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationThe filtrate thereof was concentrated under a reduced pressure
  9. additionTo the residue was added diethyl ether
  10. concentrationconcentrated under a reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-a723405ee919492cbb5c36d5b9d41df6
Quelldatensatz
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08058444B2

Notizen zur Reaktion

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