Reaktion #1076738

Reaktionsgleichung

2,3,3-trimethylindolenine

3-iodopropionic acid

→

N-(2-carboxyethyl)-2,3,3-trimethylindolinium iodide

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeA 2-necked 50 milliliter round-bottomed flask equipped with a magnetic stirring bar and an argon inlet
2. 2
   workup.ADDITIONwas charged
3. 3
   Sonstigeprecipitated out of solution
4. 4
   Sonstigeformed a highly viscous medium
5. 5
   TemperaturUpon cooling
6. 6
   Extraktionthe reaction mixture was extracted three times with 200 milliliter portions of diethyl ether
7. 7
   Sonstigeto remove all of the
8. 8
   workup.DISSOLUTIONThe remaining crystalline solid was then dissolved in 10 milliliters of water
9. 9
   Extraktionextracted three times with 50 milliliter portions of diethyl ether
10. 10
    Extraktionextracted three times with 25 milliliter portions of CHCl3
11. 11
    SonstigeThe aqueous layer was then removed
12. 12
    Sonstigedried under vacuum (1.0 mm Hg) for 24 hours
13. 13
    SonstigeThe resulting amorphous solid was then recrystallized from toluene/CHCl3

Vorschrift

A 2-necked 50 milliliter round-bottomed flask equipped with a magnetic stirring bar and an argon inlet was charged with re-distilled (pressure 2 mm Hg, temperature 45° C.) 2,3,3-trimethylindolenine (7.95 grams, 50.0 mmol) and 3-iodopropionic acid (2.00 grams, 10 mmol). The mixture was heated to 80° C. for 12 hours, during which time the product precipitated out of solution and formed a highly viscous medium. Upon cooling, the reaction mixture was extracted three times with 200 milliliter portions of diethyl ether to remove all of the unreacted starting material. The remaining crystalline solid was then dissolved in 10 milliliters of water, extracted three times with 50 milliliter portions of diethyl ether, and extracted three times with 25 milliliter portions of CHCl3. The aqueous layer was then removed and dried under vacuum (1.0 mm Hg) for 24 hours. The resulting amorphous solid was then recrystallized from toluene/CHCl3 mixtures to produce the N-(2-carboxyethyl)-2,3,3-trimethylindolinium iodide product as 3.0 grams of a yellow solid (83.5 percent yield). 1H and 13C NMR spectra indicated the following:

Quelle