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Benzene → Diethyl (pyridin-4-ylmethyl)phosphonate

HRID 1615207
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1615207
[P:1]([O-:9])([O:6][CH2:7][CH3:8])([O:3][CH2:4][CH3:5])=O.Cl[C:11]1[CH:16]=[CH:15][N:14]=[CH:13][CH:12]=1.[CH:17]1C=CC=CC=1>>[N:14]1[CH:15]=[CH:16][C:11]([CH2:17][P:1](=[O:9])([O:3][CH2:4][CH3:5])[O:6][CH2:7][CH3:8])=[CH:12][CH:13]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 241Benzene2×HCID 122884-ChloropyridineHCID 5166299Diethyl phosphoric acid

Produkt 1

HCID 10078602Diethyl (pyridin-4-ylmethyl)phosphonate

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

To a suspension of 4-chloropyridine hydrochloride (3.28 g, 20 mmol) in benzene (50 mL) was added 40% NaOH (1.35 mL). The resulting mixture was sonicated for 10 min and filtered. The residue was treated with additional benzene (15 mL), sonicated and filtered. The combined benzene layers were dried (Na2SO4) to give a solution of 4-chloropyridine which was used without further characterization (vida infra). A solution of diethyl phosphate (3.03 g, 22 mmol) in benzene (35 mL) was treated with freshly cut Na (510 mg, 22 mmol). The resulting mixture was refluxed for 30 min (oil temp. 90° C.), cooled to 0° C., then treated added dropwise over 10 min. with the solution of 4-chloropyridine in benzene (prepared as described above). After addition, the resulting mixture was refluxed for 3 h (oil temp. 100° C.) under argon then cooled to rt. The insoluble white precipitate was removed by filtration and rinsed with benzene (20 mL). The combined filtrate was concentrated and dried under high vacuum to give 3.5 g of diethyl pyridin-4-ylmethylphosphonate as a colorless liquid.

Aufarbeitung

  1. temperaturecooled to 0° C.
  2. additiontreated
  3. additionAfter addition
  4. temperaturethe resulting mixture was refluxed for 3 h (oil temp. 100° C.) under argon
  5. temperaturethen cooled to rt
  6. customThe insoluble white precipitate was removed by filtration
  7. washrinsed with benzene (20 mL)
  8. concentrationThe combined filtrate was concentrated
  9. customdried under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-47196e38e9104dec8898178516d96476
Quelldatensatz
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08765748B2

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