Réaction #346534

Équation de réaction

magnesium

phosphorus pentoxide

magnesium

acridone

p-bromostyrene

→

9-(p-vinylphenyl)acridine

Rendement 42.1%

Solvants

benzene

tetrahydrofuran

tetrahydrofuran

tetrahydrofuran

Conditions de réaction

Traitement

1. 1
   AutreInto a four-neck flask equipped with a stirrer, a nitrogen gas inlet tube, a reflux condenser with a calcium chloride tube and a dropping funnel
2. 2
   workup.ADDITIONwas added dropwise
3. 3
   Températureunder gentle reflux in a dry nitrogen gas stream
4. 4
   workup.ADDITIONwas added dropwise over a period of two hours
5. 5
   TempératureAfter refluxing for further 5 hours
6. 6
   Températureto cool
7. 7
   workup.ADDITIONpoured onto hydrochloric acid-ice
8. 8
   Autrehydrolysis
9. 9
   ExtractionThe organic layer was extracted with ether
10. 10
    Séchagethe extract was dried over anhydrous sodium sulfate
11. 11
    workup.DISTILLATIONThe solvent was then distilled off
12. 12
    Autreto obtain a yellow semi-solid
13. 13
    workup.STIRRINGThe mixture was stirred at room temperature for 5 hours
14. 14
    AutreThe supernatant liquid separated by decantation
15. 15
    Lavagewas washed with water
16. 16
    Autredried
17. 17
    Concentrationconcentrated to dryness
18. 18
    AutreThe residue was purified by silica gel chromatography

Mode opératoire

Into a four-neck flask equipped with a stirrer, a nitrogen gas inlet tube, a reflux condenser with a calcium chloride tube and a dropping funnel were charged 4.9 g of magnesium cut powder and 50 ml of tetrahydrofuran. 36.6 Grams of p-bromostyrene diluted with tetrahydrofuran to about 4 times the weight was added dropwise under gentle reflux in a dry nitrogen gas stream. After the magnesium had disappeared, a solution consisting of 37.0 g of acridone and 600 ml of tetrahydrofuran was added dropwise over a period of two hours with stirring. After refluxing for further 5 hours, the reaction mixture was allowed to cool and then poured onto hydrochloric acid-ice to effect hydrolysis. The organic layer was extracted with ether and the extract was dried over anhydrous sodium sulfate. The solvent was then distilled off to obtain a yellow semi-solid. Almost the same weight (60 g) of phosphorus pentoxide was added to 500 ml of a solution of the semi-solid in benzene. The mixture was stirred at room temperature for 5 hours and then allowed to stand overnight. The supernatant liquid separated by decantation was washed with water, dried, and then concentrated to dryness. The residue was purified by silica gel chromatography to obtain 22.5 g of 9-(p-vinylphenyl)acridine. Yield 42.1%.

Source