Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199170Generated: October 25, 2026

Maleic Anhydride → Levopimaric acid

https://huagongshe.com/reaction/2199170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AnhydrideHCID 7923—
ReactantAbietic AcidHCID 10569—
Reactant(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-phenylprop-2-enoxy]oxane-3,4,5-triolHCID 5280656—
SolventAcetic AcidHCID 176—
ProductLevopimaric acidHCID 221062—

Reaction Conditions

Temperature120 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09357775B2
Source datasetuspto-grants-2016_06
ORD IDord-4bace5f2f507489a963b1c19518747f2
Source noteuspto-grants-2016_06