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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 625204Erstellt: 25. Oktober 2026

Diphenyl Ether → Di-n-octylphosphinic acid

https://huagongshe.com/reaction/625204

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiphenyl EtherHCID 7583—
EduktTrioctylphosphineHCID 20851—
EduktTrioctylphosphine oxideHCID 65577—
EduktOleic AcidHCID 445639—
EduktOleylamineHCID 5356789—
EduktSeleniumHCID 6326970—
LösungsmittelMethanolHCID 887—
LösungsmittelTolueneHCID 1140—
LösungsmittelAcetonitrileHCID 6342—
Lösungsmittel1-OctadeceneHCID 8217—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktDi-n-octylphosphinic acidHCID 99411—

Reaktionsschritte

Materials. 1-methyl-2-pyrrolidinone (99.5%, Aldrich), 1-octadecene (90%, Aldrich), acetonitrile (99.9%, Fisher Chemical), BiCl3 (99.999%, Strem), CdO (99.5%, Aldrich), diphenyl ether (99%, Aldrich), methanol (ACS grade, VWR), oleic acid (90%, Aldrich), oleylamine (70% Aldrich), selenium (99.99%, Strem), trioctylphosphine (90%, Aldrich), trioctylphosphine oxide (99%, Strem), toluene (ACS grade, VWR). 0.1M Se-ODE was prepared by dissolving selenium powder in 1-octadecene at 180° C. for 5 hr under inert atmosphere according to the procedure by Bullen et al. [42]; trioctylphosphine oxide (TOPO) was recrystallized from acetonitrile prior to use; di-n-octylphosphinic acid (DOPA) was synthesized according to the procedure reported by Wang et al. [1], a stock suspension of 2 mM BiCl3 in NMP was prepared in advance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09306110B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-cb7f6477f1344635a0b17cb21d123fc0
Quellennotizuspto-grants-2016_04