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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895758Generated: October 25, 2026

Imidazole → Imidazole trimellitate

https://huagongshe.com/reaction/895758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTrimellitic acidHCID 10708—
ReactantGlycidoxypropyltrimethoxysilaneHCID 17317—
ReactantSilaneHCID 23953—
Reactant2-PhenylimidazoleHCID 69591—
ProductImidazole trimellitateHCID 22381556—

Reaction Steps

13.62 g (0.2 mol) of imidazole was melted at 95° C., and 47.27 g (0.2 mol) of (3-glycidoxypropyl)trimethoxysilane was added dropwise thereto over a period of 30 minutes while stirred in an argon atmosphere. Following addition, the product was further reacted for one hour at a temperature of 95° C., yielding an imidaz,ole group-containing silane coupling agent comprising a mixture of the compounds represented by the chemical formulas (1), (2), and (3) below. In the formulas (1), (2), and (3) below, R1, R2, and R3 are H; R4 is CH3; n is 3; and m is 3. 2.16 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 continues for one hour, and the product was cooled to room temperatures, 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. 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916865B2
Source datasetuspto-grants-2005_07
ORD IDord-784e364f680f4d0fbdd8a79623139bc2
Source noteuspto-grants-2005_07