Reaktion #1552041

Reaktionsgleichung

1-(3-dimethylamino propyl)-3-ethyl carbodiimide hydrochloride

phenylalanine

2-(phenylseleno)ethanol

THF

→

N-acetylphenylalanine 2-(phenylseleno)ethyl ester

Lösungsmittel

ethyl acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   Extraktionextracted with 50 ml of a 0.5 M HCl solution
2. 2
   TrocknenThe organic phase was dried over sodium sulfate
3. 3
   Filtrationfiltered
4. 4
   Sonstigethe solvent was removed in vacuo
5. 5
   SonstigePurification by column chromatography (PE:EE=2:1)
6. 6
   Sonstigeyielded 2.9 g (91% of th., 98% of lit.) of a yellowish liquid

Vorschrift

In a 50 ml round bottomed flask, 2.55 g (13.3 mmol) of 1-(3-dimethylamino propyl)-3-ethyl carbodiimide hydrochloride and 1.7 g of (8.2 mmol) phenylalanine were added to a solution of 1.87 g (9.3 mmol) of 2-(phenylseleno)ethanol in 20 ml of THF. The reaction mixture was then stirred for 12 hours at room temperature. The mixture was then diluted with 50 ml of ethyl acetate and extracted with 50 ml of a 0.5 M HCl solution. The organic phase was dried over sodium sulfate, filtered, and the solvent was removed in vacuo. Purification by column chromatography (PE:EE=2:1) yielded 2.9 g (91% of th., 98% of lit.) of a yellowish liquid.

Quelle