Réaction #685009

Équation de réaction

(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

Solvants

acetic acid

Conditions de réaction

Traitement

1. 1
   Autreprepared
2. 2
   Températurethe mixture is heated
3. 3
   Températureto reflux for 15 h
4. 4
   AutreThe solvent is evaporated in vacuo
5. 5
   workup.DISSOLUTIONthe residual material is dissolved in ethyl acetate (20 mL)
6. 6
   LavageThe organic solution is washed with a saturated aqueous solution of NaHCO3 (5 mL), water (5 mL)
7. 7
   Séchagebrine (5 mL), dried (Na2SO4)
8. 8
   Filtrationfiltered
9. 9
   Concentrationconcentrated in vacuo
10. 10
    Filtrationfiltered

Mode opératoire

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).

Source