Dichloromethane → Dibutyl 2-methylpropyl phosphate

HRID 1383253Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1383253
[P:1](Cl)([O:8][CH2:9][CH2:10][CH2:11][CH3:12])([O:3][CH2:4][CH2:5][CH2:6][CH3:7])=[O:2].ClCCl.[CH2:17]([OH:21])[CH:18]([CH3:20])[CH3:19]>N1C=CC=CC=1>[P:1]([O:21][CH2:17][CH:18]([CH3:20])[CH3:19])([O:8][CH2:9][CH2:10][CH2:11][CH3:12])([O:3][CH2:4][CH2:5][CH2:6][CH3:7])=[O:2]

Komponenten

5

Versuchsvorschrift

A solution of di-n-butyl chlorophosphate (130.3 g, 0.57 mole) in 600 mL of dichloromethane containing 55.37 g (0.70 mole) of pyridine was cooled to 0° C. Isobutanol (42.25 g, 0.57 mole) was added dropwise over 1 hour. The formation of a white precipitate was immediately observed. The reaction mixture was then stirred for 24 hours at room temperature. The pyridinium hydrochloride was filtered off, and the solution was washed with water (2×250 mL), aqueous 0.5 N HCl (2×250 mL) and water (25×250 mL). The organic phase was dried over anhydrous magnesium sulfate for 12 hours. Filtration of the drying agent, followed by the removal of the solvent using a Roto-vap, yielded di-n-butyl isobutyl phosphate as a clear colorless liquid. Distillation of the crude product (68° C. at 0.02 torr) gave 125 g of 94.8% di-n-butyl isobutyl phosphate (DBIBP).

Aufarbeitung

  1. filtrationThe pyridinium hydrochloride was filtered off
  2. washthe solution was washed with water (2×250 mL), aqueous 0.5 N HCl (2×250 mL) and water (25×250 mL)
  3. dry with materialThe organic phase was dried over anhydrous magnesium sulfate for 12 hours
  4. filtrationFiltration of the drying agent
  5. customfollowed by the removal of the solvent

Quellen und Nachweise

ORD-Eintrag
ord-5c2e8e0b4c194bfb87376bfe213cfd0a
Quelldatensatz
uspto-grants-2001_07
Patentnummer
US06254799B1

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