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HRID 637549作成日:2026年10月25日

Benzene → 3,3'-Diaminobenzophenone

https://huagongshe.com/reaction/637549

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物Potassium CarbonateHCID 11430—
反応物3,3'-Dinitro-4-chloro-4'-fluoro benzophenoneHCID 22987185—
反応物HCID 178418361HCID 178418361—
触媒Trioctylmethylammonium chlorideHCID 21218—
触媒PalladiumHCID 23938—
溶媒Hydrochloric AcidHCID 313—
生成物3,3'-DiaminobenzophenoneHCID 69145104.3%

反応手順

To a closed glass vessel equipped with a thermometer and a stirrer, there are added 49 g (0.15 moles) of 3,3'-dinitro-4-chloro-4'-fluoro benzophenone, 1 g of palladium black catalyst and 300 ml of benzene. While the mixture being stirred at 65°-70° C., 20.2 l (0.9 moles) of hydrogen is absorbed therein during about 6 hours. Then, after there are added 180 g (0.45 moles) of 35% aqueous solution of potassium carbonate and 3 g of 90% aqueous solution of trioctylmethyl ammonium chloride (available from Tokyo-Kasei Co.), additional hydrogen, 7.4 l (0.33 moles), is introduced during about 5 hours while the mixture being stirred at 65°-70° C. The mixture at that temperature is filtered to remove the catalyst. Organic phase is separated from the filtrate, added with magnesium sulfate for removing water and then blown with dry hydrochloric gas to saturation. The precipitate thus obtained is filtered, washed with 50 ml of benzene and dried to obtain 33.2 g (yield 77.7%) of 3,3'-diamino benzophenone in the hydrochloric acid salt form. Recrystallization from 20% aqueous isopropyl alcohol gives pure compound, as slightly yellow needle-like crystals. M.P. 265°-267° C. (decomposed).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04556738
出典データセットuspto-grants-1985_12
ORD IDord-04b3a5dbfc8645a28e4e89f16160a1f7
出典メモuspto-grants-1985_12