Reacción #9379

Ecuación de reacción

AlCl3

Thionyl chloride

2,3-dichloro-benzoic acid

benzene

→

6,7-dichloro-1-indanone

Rendimiento 80.0%

Disolventes

dichloroethane

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturato reflux until no more gas evolution
2. 2
   Concentraciónwas concentrated
3. 3
   workup.ADDITIONThe concentrate was diluted with dichloroethane
4. 4
   OtroEthylene was bubbled through the mixture for 4 h
5. 5
   Otroquenched with 4 N HCl
6. 6
   OtroThe resulting layers were separated
7. 7
   Extracciónthe aqueous layer was extracted with Et2O (3×250 mL)
8. 8
   LavadoThe combined organic extracts were washed with H2O (3×150 mL), saturated NaHCO3 (3×150 mL), brine (1×150 mL)
9. 9
   Secadodried over MgSO4
10. 10
    Concentraciónconcentrated
11. 11
    workup.ADDITIONThe concentrate was added to a slurry of AlCl3 (9.0 g) and NaCl (2.4 g) at 130° C
12. 12
    workup.STIRRINGThe resulting mixture was stirred at 180° C. for 2 hours after which it
13. 13
    Temperaturawas cooled to room temperature
14. 14
    Otroquenched with ice
15. 15
    ExtracciónThe mixture was extracted with CH2Cl2 (3×500 mL)
16. 16
    Concentraciónthe combined organic extracts were concentrated
17. 17
    Otropurified by column chromatography

Procedimiento

Thionyl chloride (5.73 mL, ˜79 mmol) and 2,3-dichloro-benzoic acid (commercially available from Aldrich) (10.0 g, 52.4 mmol) in benzene was heated to reflux until no more gas evolution was observed. After cooling to rt the mixture was concentrated. The concentrate was diluted with dichloroethane and added to AlCl3 (7.0 g, ˜53 mmol) in dichloroethane at 10–20° C. Ethylene was bubbled through the mixture for 4 h. The mixture was stirred overnight and quenched with 4 N HCl. The resulting layers were separated and the aqueous layer was extracted with Et2O (3×250 mL). The combined organic extracts were washed with H2O (3×150 mL), saturated NaHCO3 (3×150 mL), brine (1×150 mL), dried over MgSO4 and concentrated. The concentrate was added to a slurry of AlCl3 (9.0 g) and NaCl (2.4 g) at 130° C. The resulting mixture was stirred at 180° C. for 2 hours after which it was cooled to room temperature and quenched with ice followed by concentrated HCl. The mixture was extracted with CH2Cl2 (3×500 mL) and the combined organic extracts were concentrated and purified by column chromatography using 20% EtOAc:hexane eluant to give 6.8 g (80%) of 6,7-dichloro-1-indanone. Use of 6,7-dichloro-indan-1-one in Method NINETEEN produced 4-(4,5-dichloro-indan-2-yl)-1,3-dihydro-imidazole-2-thione (Compound 153).

Fuente