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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129456생성일: 2026년 10월 24일

p-Toluenesulfonic acid → 9-(2,2-Bis(4-chlorophenyl))ethoxy-9H-indeno[1,2-b]pyrazine-2,3(1H, 4H)-dione

https://huagongshe.com/reaction/129456

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물4-Chloro-beta-(4-chlorophenyl)benzeneethanolHCID 17533—
반응물9-Hydroxy-9H-indeno[1,2-b]pyrazine-2,3(1H,4H)-dioneHCID 19035985—
용매Acetic AcidHCID 176—
생성물9-(2,2-Bis(4-chlorophenyl))ethoxy-9H-indeno[1,2-b]pyrazine-2,3(1H, 4H)-dioneHCID 5374381617.5%

반응 단계

A suspension of 9-hydroxy-9H-indeno[1,2-b]pyrazine-2,3(1H, 4H)-dione. 1H2O (0.50 g, 2.13 mmol) in acetic acid (30 ml), 2,2-bis(4-chlorophenyl)ethanol (2.84 g, 10.65 mmol) and p-toluensulfonic acid (20 mg) was refluxed for 21 hours. The reaction mixture was evaporated in vacuo to dryness, the residue was suspended in ethanol (40 ml) and the precipitate was filtered off and washed with ethanol and dried to give 0.39 g of the crude product, which was recrystallized from ethanol to yield 0.174 g (17.5%) of the title compound. M.p. 234°-237° C. 1H-NMR (DMSO-d6, δ): 3.68 (t, 1H), 4.0 (t, 1H), 4.27 (t, 1H), 5.23 (s, 1H), 7.1-7.5 (m, 12H), 11.98 (s, 1H), 12.25 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05468748
출처 데이터셋uspto-grants-1995_11
ORD IDord-86446b81494e404a84c039341f23ae1b
출처 메모uspto-grants-1995_11