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Potassium Iodide → N-butyl-3,3-bis(diethoxyphosphinyl)propionamide

HRID 1972
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1972
[CH2:1]([P:10](=[O:17])([O:14][CH2:15][CH3:16])[O:11][CH2:12][CH3:13])[P:2](=[O:9])([O:6][CH2:7][CH3:8])[O:3][CH2:4][CH3:5].[H-].[Na+].[H-].[CH2:21]([NH:25][C:26](=[O:29])[CH2:27]Cl)[CH2:22][CH2:23][CH3:24].[I-].[K+].[Cl-].[Na+]>C1COCC1>[CH2:21]([NH:25][C:26](=[O:29])[CH2:27][CH:1]([P:2]([O:6][CH2:7][CH3:8])([O:3][CH2:4][CH3:5])=[O:9])[P:10]([O:11][CH2:12][CH3:13])([O:14][CH2:15][CH3:16])=[O:17])[CH2:22][CH2:23][CH3:24]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 6

HCID 4875Potassium IodideHCID 5234Sodium ChlorideHCID 15455Tetraethyl methylenediphosphonateHCID 24758Sodium hydrideHCID 166653HydrideHCID 219645N-butyl-2-chloroacetamide

Produkt 1

HCID 19689044
N-butyl-3,3-bis(diethoxyphosphinyl)propionamide
Ausbeute 70 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel3×

Versuchsvorschrift

Tetraethyl methylenebisphosphonate (1.44 g, 5.0 mmol) in THF (1 mL) was added to a slurry of 80% sodium hydride (150 mg, 5.0 mmol) in THF (4 mL) at 0° C. The reaction was warmed to room temperature and stirred until all of the hydride was consumed. A solution of N-butyl-2-chloroacetamide (0.75 g, 5.0 mmol) in THF (1 ml) and potassium iodide (100 mg) were then added. The reaction mixture was then heated at 50° C. for 18 hours, during which time sodium chloride precipitated. Additional sodium hydride (20 mg) was added, and the reaction mixture was heated an additional 4 hours. After cooling, the mixture was poured into 1N HCl (10 mL) and diethyl ether (50 mL) was added. The diethyl ether layer was further extracted with water (3×10 mL). The combined aqueous fractions were extracted with dichloromethane (4×25 mL). The combined extracts were dried (Na2SO4) and concentrated to give the title compound (1.40 g, 70%) as an oil.

Aufarbeitung

  1. customwas consumed
  2. customprecipitated
  3. additionAdditional sodium hydride (20 mg) was added
  4. temperaturethe reaction mixture was heated an additional 4 hours
  5. temperatureAfter cooling
  6. additionthe mixture was poured into 1N HCl (10 mL) and diethyl ether (50 mL)
  7. additionwas added
  8. extractionThe diethyl ether layer was further extracted with water (3×10 mL)
  9. extractionThe combined aqueous fractions were extracted with dichloromethane (4×25 mL)
  10. dry with materialThe combined extracts were dried (Na2SO4)
  11. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-0d06fa7cb400433aac9523d5cb4e75c0
Quelldatensatz
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05728650

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