Reacción #2018

Ecuación de reacción

ethyl acetate

allyl alcohol

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

EDC

→

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

Disolventes

—

hexanes

methylene chloride

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrothe resulting homogeneous solution quenched with water
2. 2
   Extracciónextracted with methylene chloride
3. 3
   LavadoThe methylene chloride layer was washed with 5% aqueous citric acid
4. 4
   SecadoThe methylene chloride layer was dried over anhydrous magnesium sulfate powder
5. 5
   Filtraciónfiltered
6. 6
   Otroevaporated under reduced pressure
7. 7
   Otroto give an oil
8. 8
   Otroafforded the product (408 mg; 60%) as a pale yellow gum

Procedimiento

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).

Fuente