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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1397645Erstellt: 26. Oktober 2026

Maleic Anhydride → Levopimaric acid

https://huagongshe.com/reaction/1397645

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMaleic AnhydrideHCID 7923—
EduktAbietic AcidHCID 10569—
Edukt(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-phenylprop-2-enoxy]oxane-3,4,5-triolHCID 5280656—
LösungsmittelAcetic AcidHCID 176—
ProduktLevopimaric acidHCID 221062—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Example 1 describes the preparation of quaternary ammonium-containing rosin acids and rosin esters, according to the exemplary method shown in FIG. 1. The synthesis for the integration of quaternary ammonium group into the moiety of rosin is described as follows: The abietic acid, maleic anhydride and acetic acid were mixed in a round bottom flask under a nitrogen atmosphere and heated at 120° C. for 12 h to yield levopimaric acid. The levopimaric acid is stirred with dimethylethylenediamine at 85° C. for 8 h, yielding a rosin-derived tertiary ammonium derivative, which is then stirred with an alkyl halide (e.g. bromoethane, bromohexane, bromooctane and bromododecane) at 40° C. in tetrahydrofuran for 48 h to yield quaternary ammonium-containing rosin acid 1. The quaternary ammonium-containing rosin acid is dissolved in thionyl chloride and refluxed for 12 h. Then, thionyl chloride is removed by reduced pressure distillation. Ethanol, triethylamine and tetrahydrofuran are added and stirred at room temperature for 24 h to yield the ethyl ester of quaternary ammonium-containing rosin acid 2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08901245B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-45bced8c7d1a46cf86d75b735a678ccb
Quellennotizuspto-grants-2014_12