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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68181생성일: 2026년 10월 24일

Acetone → Anthra[2,3-b]benzo[d]thiophene-7,12-dione

https://huagongshe.com/ko/reaction/68181

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Phosphorus pentachlorideHCID 24819—
반응물2-(Dibenzothiophene-2-ylcarbonyl)benzoic acidHCID 4346778—
반응물Aluminum(III) ChlorideHCID 6451240—
용매1,2-DichlorobenzeneHCID 7239—
생성물Anthra[2,3-b]benzo[d]thiophene-7,12-dioneHCID 28227116.1%

반응 조건

온도140 °C

반응 단계

To a mixture of 2-(o-carboxybenzoyl)dibenzothiophene (35.6 g, 107 mmol) and phosphorus pentachloride (33.5 g, 161 mmol) in anhydrous 1,2-dichlorobenzene (430 cm3) is added aluminum chloride (21.4 g, 161 mmol). The mixture is then heated at 140° C. for 17 hours. The reaction mixture cooled to 23° C. and the solvent removed under vacuum to give a black solid. Acetone (500 cm3) is added and the mixture filtered to give a green/yellow solid which is dried under vacuum. To the solid is added dichloromethane (1000 cm3) and the mixture heated. The hot mixture is passed through a very short plug of silica (dichloromethane) to give anthra[2,3-b]benzo[d]thiophene-7,12-dione as a yellow solid (5.43 g, 16%). MS m/z 314 (M+). 1H NMR (300 MHz, CDCl3) 9.04 (s, 1H), 8.73 (s, 1H), 8.31-8.41 (m, 3H), 7.86-7.93 (m, 1H), 7.78-7.85 (m, 2H), 7.50-7.61 (m, 2H); 13C NMR (75 MHz, CDCl3) 183.1, 182.8, 145.3, 141.3, 139.9, 134.7, 134.2, 134.1, 133.9, 133.8, 131.1, 129.9, 128.8, 127.4, 125.5, 123.2, 123.1, 122.4, 120.8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08821762B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-af71c4cef0c54ebba9e4ea060a3da89e
출처 메모uspto-grants-2014_09