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HRID 263913作成日:2026年10月25日

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/263913

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物4-Chloro-beta-(4-chlorophenyl)benzeneethanolHCID 17533—
反応物9-Hydroxy-9H-indeno[1,2-b]pyrazine-2,3(1H,4H)-dioneHCID 19035985—
溶媒Acetic AcidHCID 176—
生成物9-(2,2-Bis(4-chlorophenyl))ethoxy-9H-indeno[1,2-b]pyrazine-2,3(1H, 4H)-dioneHCID 5374381617.5%

反応手順

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. 1 -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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646146
出典データセットuspto-grants-1997_07
ORD IDord-19fd8a0ddc62483d986376d860a55d3c
出典メモuspto-grants-1997_07