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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895759Generated: October 27, 2026

Imidazole → Imidazole trimellitate

https://huagongshe.com/reaction/895759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTrimellitic acidHCID 10708—
Reactant3-(Trimethoxysilyl)propyl methacrylateHCID 17318—
ReactantSilaneHCID 23953—
Reactant2-PhenylimidazoleHCID 69591—
SolventEthyl AcetateHCID 8857—
ProductImidazole trimellitateHCID 22381556—

Reaction Steps

13.6 g (0.2 mol) of imidazole and 24.8 g (0.1 mol) of (3-methacryloxypropyl)trimethoxysilane were mixed and reacted at 100° C. for 11 hours. After cooling to room temperature, 100 ml of ethyl acetate was added, and excess imidazole was removed by washing the product three times in 100 ml of deionized water. Molecular sieves were added to the product, and the ethyl acetate solution was dried overnight. Subsequently, the ethyl acetate was distilled off in a rotary evaporator, and the imidazole group-containing silane coupling agent expressed by the formula (4) below was obtained. In the formula, R6, R7, and R8 are H; R9 is CH3; R10 is CH3; o is 3; and p is 3. 12.64 g (0.04 mol) of the imidazole group-containing silane coupling agent thus obtained, 8.64 g (0.06 mol) of 2-phenylimidazole (melting point: 137-147° C.), and 21.0 g (0.1 mol) of trimellitic acid were heated and mixed at 160° C., the reaction was continued for one hour, and the product was cooled to room temperature, yielding an imidazole trimellitate composition that was solid at normal temperature. The solid product thus obtained was ground with a mortar and classified by a sieve with hole openings of 90 microns to yield pulverized Sample No. 2. Evaluation of Adhesion Properties

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916865B2
Source datasetuspto-grants-2005_07
ORD IDord-f49c0bf7e3e54140a1fa1894069f6279
Source noteuspto-grants-2005_07