Реакция #155363

ord-af71c4cef0c54ebba9e4ea060a3da89e

Уравнение реакции

CC(C)=O
Acetone
O=C(O)c1ccccc1C(=O)c1ccc2sc3ccccc3c2c1
2-(o-carboxybenzoyl)dibenzothiophene
ClP(Cl)(Cl)(Cl)Cl
phosphorus pentachloride
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
O=C1c2ccccc2C(=O)c2cc3c(cc21)sc1ccccc13
anthra[2,3-b]benzo[d]thiophene-7,12-dione
Выход 16.1%

Растворители

Условия реакции

Температура
140°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction mixture cooled to 23° C.
  2. 2
    Другоеthe solvent removed under vacuum
  3. 3
    Другоеto give a black solid
  4. 4
    Фильтрацияthe mixture filtered
  5. 5
    Другоеto give a green/yellow solid which
  6. 6
    Другоеis dried under vacuum
  7. 7
    workup.ADDITIONTo the solid is added dichloromethane (1000 cm3)
  8. 8
    Температураthe mixture heated

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08821762B2uspto-grants-2014_09