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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289261Generated: October 29, 2026

Phthalic Anhydride → Glycidyl neodecanoate

https://huagongshe.com/reaction/1289261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantMethylhydroquinoneHCID 7253—
ReactantMaleic AnhydrideHCID 7923—
ReactantTriethylene GlycolHCID 8172—
Reactant4-Methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dioneHCID 12726603—
SolventDiethylene GlycolHCID 8117—
ProductGlycidyl neodecanoateHCID 33600—

Reaction Conditions

Temperature205 °C

Reaction Steps

593 parts of triethylene glycol, 206 parts of diethylene glycol, 305 parts of phthalic anhydride, 490 parts of 3-methyltetrahydrophthalic anhydride and 0.158 parts of toluhydroquinone were placed in a 2 liter flask containing four openings equipped with a thermometer, stirrer, inert gas introduction opening, and reflux condenser, respectively. The mixture was heated to 205° C. under a nitrogen atmosphere and allowed to react for 15 hours; upon reaching a solid acid value of 15, the mixture was cooled to 120° C. followed by addition of 87 parts of maleic anhydride. The temperature was then raised to 190° C. and allowed to react for 5 hours until reaching a solid acid value of 24, at which point it was cooled to 160° C. After 148 parts of CARDURA E-10 (an epoxy compound produced by Shell Chemicals Co., Ltd.) were added and allowed to react for 3 hours at 130° C., 1078 parts of dipropylene glycol monomethylether methacrylate were then added to produce a resin composition with a nonvolatile content of 60.0%, an acid value of 1.1 and a Gardner viscosity of S-T. 80 parts of the resin of Example 10 were then added to 20 parts of the above resin to produce a resin composition with a nonvolatile content of 60.0%, an acid value of 2.9 and a Gardner viscosity of P-Q. The resultant resin composition was then placed through the same evaluation tests as in Example 7, and the results are shown in Table 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747597
Source datasetuspto-grants-1998_05
ORD IDord-64131b7cf14a411ca8a1539fae18239c
Source noteuspto-grants-1998_05