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Pentaerythritol → Pentaerythritol, cyclic phosphate (1:1) (8CI)

HRID 2254867
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2254867
[OH:1][CH2:2][C:3]([CH2:8][OH:9])([CH2:6][OH:7])[CH2:4][OH:5].[P:10](Cl)(Cl)(Cl)=[O:11]>CC(C1C=CC(OP(OC2C=CC=CC=2)(OC2C=CC=CC=2)=O)=CC=1)C.CC(C1C=CC=C(OP(OC2C=CC=CC=2)(OC2C=CC=CC=2)=O)C=1)C.CC(C1C(OP(OC2C=CC=CC=2)(OC2C=CC=CC=2)=O)=CC=CC=1)C>[CH2:4]1[O:5][P:10]2([O:7][CH2:6][C:3]1([CH2:8][OH:9])[CH2:2][O:1]2)=[O:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 8285PentaerythritolHCID 24813Phosphorus oxychloride

Produkt 1

HCID 199942Pentaerythritol, cyclic phosphate (1:1) (8CI)Ausbeute 75 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 24832072HCID 24832072, VerbindungLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

In a 250 mL four-necked reaction flask fitted with a mechanical stirrer, pot thermometer, addition funnel, and condenser with gas outlet were placed 42.5 g (0.313 mole) of pentaerythritol and 150 mL of PHOSFLEX 41P brand of isopropylated triphenyl phosphate under nitrogen. The mixture was stirred and heated at 95° C. as 49.2 g (0.321 mole) of phosphorus oxychloride was added dropwise over five hours. The resulting white slurry was heated to 100° C. with a nitrogen gas sparge for eight hours to remove HCl. The mixture was cooled to 50° C. and filtered. The solid was washed three times with 40 mL of hexane and dried at 100° C./2 mm Hg for sixteen hours to give 42.3 g (71.2% yield) of crude pentaerythritol phosphate alcohol (2,6,7-trioxa- 1-phosphabicyclo [2.2.2]octane-4-methanol-1-oxide). The product had a 31P NMR resonance at -6.0 ppm in d6 -DMSO.

Aufarbeitung

  1. customIn a 250 mL four-necked reaction flask fitted with a mechanical stirrer
  2. additionpot thermometer, addition funnel, and condenser with gas outlet
  3. additionwas added dropwise over five hours
  4. customsparge for eight hours
  5. customto remove HCl
  6. temperatureThe mixture was cooled to 50° C.
  7. filtrationfiltered
  8. washThe solid was washed three times with 40 mL of hexane
  9. customdried at 100° C./2 mm Hg for sixteen hours

Quellen und Nachweise

ORD-Eintrag
ord-519b9d3dc15c4773ba4cc02668f28e1f
Quelldatensatz
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05237085

Notizen zur Reaktion

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