Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 3,3-dimethyl-2-oxo-2,3-dihydro-1H-indole-6-carboxylic acid | HCID 14624055 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 14624056 | HCID 14624056 | — |
Reaktionsschritte
8 g. 2,3-Dihydro-3,3-dimethyl-2-oxo-(1H)-indole-6-carboxylic acid and 1 drop of dimethylformamide were heated in 50 ml. thionyl chloride for 1 hour to the boil under reflux, the substance thereby going into solution. The thionyl chloride was removed under vacuum, the residue was suspended in dichloromethane and a solution of 1.6 ml. aniline and 2.7 ml. triethylamine in 30 ml. dichloromethane added dropwise thereto at an internal temperature of 15° C. The reaction mixture was stirred for 15 minutes at ambient temperature, the solvent was removed in a vacuum and the residue was digested with water, filtered off with suction and recrystallised from ethyl acetate. There were obtained 2.8 g. (56% of theory) of the title compound; m.p. 205-206° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05019587 |
|---|
| Quelldatensatz | uspto-grants-1991_05 |
|---|
| ORD ID | ord-69488d292d83427d827b47d552657cbf |
|---|
| Quellennotiz | uspto-grants-1991_05 |
|---|