تفاعل #2439947
ord-d2348a7ac914442798744accf77cbf5f
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1workup.ADDITIONoutside as this addition
- 2أخرىformed
- 3درجة الحرارةThe mixture was warmed to 50° C.
- 4workup.STIRRINGstirred for 15 min at that temperature
- 5أخرىThe resulting reaction mixture
- 6درجة الحرارةwas heated to 90° C.
- 7workup.STIRRINGto stir for 5 hours during which the reaction mixture
- 8درجة الحرارةThe reaction was cooled to room temperature
- 9workup.ADDITIONIce was added directly to the flask
- 10workup.STIRRINGthe contents were stirred at room temperature for 15 min
- 11ترشيحThe precipitate was collected via vacuum filtration
- 12أخرىThe crude solid was purified
- 13غسيلby washing with sat. NaHCO3(aq)
الإجراء التجريبي
AlCl3 (20.0 g, 150 mmol) was placed in a dry 200 mL round bottom flask and DMF (3.30 mL) was added dropwise at 0° C. During the addition of DMF care was taken to ensure that the reaction was allowed to vent to the outside as this addition caused an exotherm to occur. Additionally as the DMF was added a white suspension formed. This suspension was allowed to stir for 30 min at room temperature, after which 4-nitrobenzoyl chloride (2.984 g, 16 mmol) was added. The mixture was warmed to 50° C. and stirred for 15 min at that temperature. The 50° C. mixture then was treated with oxindole (2.051 g, 15 mmol). The resulting reaction mixture was heated to 90° C. and allowed to stir for 5 hours during which the reaction mixture turned from a yellowish suspension to a thick black oil. The reaction was cooled to room temperature. Ice was added directly to the flask followed by water, turning the black oil into a pale yellow/white precipitate. Concentrated HCl(aq) (3 mL) was added to the reaction and the contents were stirred at room temperature for 15 min. The precipitate was collected via vacuum filtration. The crude solid was purified by washing with sat. NaHCO3(aq) providing 5-(4-Nitro-benzoyl)-1,3-dihydro-indol-2-one as a gray solid (4.05 g, 14.4 mmol, 95%).