Reaktion #685009

Reaktionsgleichung

(2-amino-4,5-dimethylthiophen-3-yl)(4-chlorophenyl)methanone

phthalic anhydride

→

2-[3-(4-chlorobenzoyl)-4,5-dimethylthiophen-2-yl]isoindoline-1,3-dione

Lösungsmittel

acetic acid

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeprepared
2. 2
   Temperaturthe mixture is heated
3. 3
   Temperaturto reflux for 15 h
4. 4
   SonstigeThe solvent is evaporated in vacuo
5. 5
   workup.DISSOLUTIONthe residual material is dissolved in ethyl acetate (20 mL)
6. 6
   WaschenThe organic solution is washed with a saturated aqueous solution of NaHCO3 (5 mL), water (5 mL)
7. 7
   Trocknenbrine (5 mL), dried (Na2SO4)
8. 8
   Filtrationfiltered
9. 9
   Einengenconcentrated in vacuo
10. 10
    Filtrationfiltered

Vorschrift

To a solution of (2-amino-4,5-dimethylthiophen-3-yl)(4-chlorophenyl)methanone (532 mg, 2 mmol; prepared as described in U.S. Pat. No. 6,323,214) in acetic acid (15 mL) is added phthalic anhydride (360 mg, 2.4 mmol) and the mixture is heated to reflux for 15 h. The solvent is evaporated in vacuo and the residual material is dissolved in ethyl acetate (20 mL). The organic solution is washed with a saturated aqueous solution of NaHCO3 (5 mL), water (5 mL), then brine (5 mL), dried (Na2SO4), filtered, and concentrated in vacuo. The crude product is stirred for 1 h in petroleum ether (20 mL), then filtered, affording (2-[3-(4-chlorobenzoyl)-4,5-dimethylthiophen-2-yl]isoindoline-1,3-dione as a yellow powder. 1H NMR (CDCl3) δ: 2.10 (s, 3H), 2.43 (s, 3H), 7.24 (d, J=8.4 Hz, 2H), 7.64 (d, J=8.4 Hz, 2H), 7.78 (m, 4H).

Quelle