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HRID 1050433作成日:2026年10月26日

Water → Tricarbonylbenzene

https://huagongshe.com/reaction/1050433

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物AnilineHCID 6115—
反応物M-PhenylenediamineHCID 7935—
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物Trimesoyl chlorideHCID 78138—
生成物TricarbonylbenzeneHCID 21448804—

反応手順

In a nitrogen atmosphere, a 50 mL four-neck flask was charged with 3 g (11.3 mmol) of 1,3,5-benzenetricarbonyl trichloride (Tokyo Chemical Industry) and 13.3 g of NMP (Junsei Chemical Co., Ltd.), following which a solution of 0.92 g (8.48 mmol) of 1,3-phenylenediamine (DuPont K.K.) and 0.79 g (8.48 mmol) of aniline (Junsei Chemical Co., Ltd.) in 13.3 g of NMP (Junsei Chemical Co., Ltd.) was added dropwise over a period of 30 minutes at an internal temperature of 12° C. and polymerization was carried out. Following the completion of dropwise addition, the flask contents were stirred for 30 minutes at room temperature, pure water (3 g) was added dropwise, followed by another 30 minutes of stirring, after which the reaction mixture was added to 450 g of pure water, thereby effecting re-precipitation. The resulting precipitate was collected by filtration, then again dissolved in a mixed solvent of 24 g of THF (Kanto Chemical Co., Ltd.) and 1.8 g of pure water, after which the solution was added to 450 g of pure water, thereby effecting re-precipitation. The resulting precipitate was collected by filtration and dried at 150° C. for 2 hours in a vacuum desiccator, thereby giving 3.3 g of the target tricarbonylbenzene-based hyperbranched polymer (abbreviated below as “TmPDA-An”). FIG. 2 shows the 1H-NMR spectrum obtained for TmPDA-An.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09382381B2
出典データセットuspto-grants-2016_07
ORD IDord-88a9313ca4784c4493051e402f1385ab
出典メモuspto-grants-2016_07