Reaktion #9379

Reaktionsgleichung

AlCl3

Thionyl chloride

2,3-dichloro-benzoic acid

benzene

→

6,7-dichloro-1-indanone

Ausbeute 80.0%

Lösungsmittel

dichloroethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturto reflux until no more gas evolution
2. 2
   Einengenwas concentrated
3. 3
   workup.ADDITIONThe concentrate was diluted with dichloroethane
4. 4
   SonstigeEthylene was bubbled through the mixture for 4 h
5. 5
   Sonstigequenched with 4 N HCl
6. 6
   SonstigeThe resulting layers were separated
7. 7
   Extraktionthe aqueous layer was extracted with Et2O (3×250 mL)
8. 8
   WaschenThe combined organic extracts were washed with H2O (3×150 mL), saturated NaHCO3 (3×150 mL), brine (1×150 mL)
9. 9
   Trocknendried over MgSO4
10. 10
    Einengenconcentrated
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
    Temperaturwas cooled to room temperature
14. 14
    Sonstigequenched with ice
15. 15
    ExtraktionThe mixture was extracted with CH2Cl2 (3×500 mL)
16. 16
    Einengenthe combined organic extracts were concentrated
17. 17
    Sonstigepurified by column chromatography

Vorschrift

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).

Quelle