Réaction #2018

Équation de réaction

ethyl acetate

allyl alcohol

N-(t-Butoxycarbonyl)-O-benzyl-D-serine

EDC

→

N-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl Ester

Solvants

—

hexanes

methylene chloride

Conditions de réaction

Traitement

1. 1
   Autrethe resulting homogeneous solution quenched with water
2. 2
   Extractionextracted with methylene chloride
3. 3
   LavageThe methylene chloride layer was washed with 5% aqueous citric acid
4. 4
   SéchageThe methylene chloride layer was dried over anhydrous magnesium sulfate powder
5. 5
   Filtrationfiltered
6. 6
   Autreevaporated under reduced pressure
7. 7
   Autreto give an oil
8. 8
   Autreafforded the product (408 mg; 60%) as a pale yellow gum

Mode opératoire

N-(t-Butoxycarbonyl)-O-benzyl-D-serine (600 mg; 2.03 mmol) was dissolved in dry methylene chloride (5 ml), allyl alcohol (152 μl; 2.23 mmol) and DMAP (25 mg; 0.20 mmol) added and finally EDC (428.5 mg; 2.24 mmol) added to the acid. The reaction mixture was stirred at room temperature for 2.5 h and the resulting homogeneous solution quenched with water and extracted with methylene chloride. The methylene chloride layer was washed with 5% aqueous citric acid then 10% aqueous sodium carbonate solution. The methylene chloride layer was dried over anhydrous magnesium sulfate powder, filtered and evaporated under reduced pressure to give an oil. Chromatography of the oil using ethyl acetate and hexanes 1:2 v/v afforded the product (408 mg; 60%) as a pale yellow gum. FAB-MS:- Calculated for C36H33N5 335.1; found 336.1 (M+1).

Source