Reaktion #326893

Reaktionsgleichung

amide

4-iodophenylalanine amide

1,3-propane sultone

→

solid

Ausbeute 17.6%

4-iodo-N-(3-sulfopropyl)-L-phenylalanine amide

Ausbeute 17.6%

Lösungsmittel

2-butanone

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwas added
2. 2
   Temperaturat reflux for 2 hours
3. 3
   FiltrationThe solid was collected by filtration
4. 4
   Waschenwashed with acetone (2×20 mL)
5. 5
   Sonstigedried in vacuo
6. 6
   workup.STIRRINGThe suspension was stirred
7. 7
   Temperaturat reflux
8. 8
   FiltrationThe solid material was collected by filtration while the mixture
9. 9
   WaschenThe solid was washed with hot MeOH (2×10 mL)

Vorschrift

The solid (1.96 g, 5.8 mmol) was dissolved in a minimum amount of water. To the solution was added aqueous NH4OH (28-30%, 15 mL). The reaction mixture was stirred at room temperature over weekend. The solvent was removed under reduced pressure and EtOAc (15 mL) was added. The mixture was heated under reflux. The hot solution was filtered. The filtrate was cooled to room temperature and was stored in the fridge. The solid was collected by filtration, washed with EtOAc, to give 4-iodophenylalanine amide. The amide (1.3 g, 4.4 mmol) was dissolved in 15 mL of 2-butanone with a few drops of DMF before 1,3-propane sultone (560 mg, 4.9 mmol) was added. The reaction mixture was stirred at reflux for 2 hours. The mixture was cooled to room temperature. The solid was collected by filtration, washed with acetone (2×20 mL) and dried in vacuo. The solid was suspended in MeOH (25 mL) and a small amount of water (1 mL). The suspension was stirred at reflux. The solid material was collected by filtration while the mixture was still hot. The solid was washed with hot MeOH (2×10 mL). Compound CO was obtained as a white solid (320 mg).

Quelle