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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 637549생성일: 2026년 10월 24일

Benzene → 3,3'-Diaminobenzophenone

https://huagongshe.com/ko/reaction/637549

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물Potassium CarbonateHCID 11430—
반응물3,3'-Dinitro-4-chloro-4'-fluoro benzophenoneHCID 22987185—
반응물HCID 178418361HCID 178418361—
촉매Trioctylmethylammonium chlorideHCID 21218—
촉매PalladiumHCID 23938—
용매Hydrochloric AcidHCID 313—
생성물3,3'-DiaminobenzophenoneHCID 69145104.3%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04556738
출처 데이터셋uspto-grants-1985_12
ORD IDord-04b3a5dbfc8645a28e4e89f16160a1f7
출처 메모uspto-grants-1985_12