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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1447329Erstellt: 27. Oktober 2026

Lauric Acid → Nonanoic Acid

https://huagongshe.com/reaction/1447329

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLauric AcidHCID 3893—
EduktLauryl alcohol diphosphonic acidHCID 4395717—
EduktDodecane-1,1,2-triphosphonic acidHCID 20550621—
LösungsmittelPhosphoric AcidHCID 1004—
LösungsmittelDibutyl butylphosphonateHCID 6539—
ProduktNonanoic AcidHCID 8158—

Reaktionsschritte

In similar manner C9, C12, C16 and C18 extractants were prepared at 150° C. from iso-nonanoic, lauric, iso-hexadecanoic and stearic acids respectively. NMR analysis of the C12 extractant revealed that dodecane-1,1,2-triphosphonic acid was a major component of the crude product and that 1-hydroxy-1,1-dodecane diphosphonic acid was absent. When a solution of the crude C12 extractant (10 wt %) in dibutyl butylphosphonate (10 wt %) and kerosene (80 wt %) was shaken with equal volume of 10 M phosphoric acid, the total carbon in the phosphoric acid was 0.01%. The same amount of carbon was found when a 10 wt % kerosene solution of dibutyl butyl phosphonate was used instead. These results indicate that loss of material from the crude C12 extractant during contact with phosphoric acid is negligible. A C12 extractant was also made from lauric acid by reaction at 110° C. for 16 h. The main component of this acid extractant was 1-hydroxy-1,1 -dodecanediphosphonic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04316877
Quelldatensatzuspto-grants-1982_02
ORD IDord-74634f1cc7ae49c980958fde48f33f85
Quellennotizuspto-grants-1982_02