Acetamidomalonic acid diethyl ester → Phenylalanine,N-acetyl--phenyl-

To a solution (1.25 M) of diethyl acetamidomalonate (10.94 g, 50.57 mmol) in N-methyl-2-pyrrolidone (40 mL) was added potassium t-butoxide (5.90 g, 52.60 mmol), and the mixture was stirred at room temperature for 1 hr. Diphenylmethylene bromide (10.0 g, 46.46 mmol) was added, and the mixture was stirred at 70° C. for 5 hrs. After completion of the reaction, 2M aqueous sodium hydroxide solution (45 mL) was added to the reaction mixture, and the mixture was stirred at 70° C. for 3 hrs. The reaction mixture was allowed to cool to room temperature, toluene (19 mL) was added, and the mixture was partitioned. The aqueous layer was adjusted to pH 7.0 with concentrated hydrochloric acid (8.8 mL). Ethyl acetate (80 mL) was added, and then concentrated hydrochloric acid (13.0 mL) was added. The mixture was partitioned, and the aqueous layer was extracted with ethyl acetate (40 mL). The organic layers were combined, successively washed with 2M hydrochloric acid (40 mL, three times) and saturated brine (10 mL), and concentrated. Toluene (30 mL) was added to the concentrated solution and the mixture was concentrated at 50° C. Toluene (30 mL) was added again, and the mixture was stirred for 30 min and cooled to 0° C. over 5 hrs, which resulted in the precipitation of white crystals. The crystals were collected by filtration and dried under reduced pressure to give the title compound (9.18 g).

1. stirringthe mixture was stirred at 70° C. for 5 hrs
2. additionwas added to the reaction mixture
3. stirringthe mixture was stirred at 70° C. for 3 hrs
4. temperatureto cool to room temperature
5. customthe mixture was partitioned
6. additionEthyl acetate (80 mL) was added
7. additionconcentrated hydrochloric acid (13.0 mL) was added
8. customThe mixture was partitioned
9. extractionthe aqueous layer was extracted with ethyl acetate (40 mL)
10. washsuccessively washed with 2M hydrochloric acid (40 mL, three times) and saturated brine (10 mL)
11. concentrationconcentrated
12. additionToluene (30 mL) was added to the concentrated solution
13. concentrationthe mixture was concentrated at 50° C
14. additionToluene (30 mL) was added again
15. stirringthe mixture was stirred for 30 min
16. temperaturecooled to 0° C. over 5 hrs
17. customwhich resulted in the precipitation of white crystals
18. filtrationThe crystals were collected by filtration
19. customdried under reduced pressure

ORD-Eintrag

ord-51905b8b82564f2c890b834a649960ae

Quelldatensatz

uspto-grants-2008_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07427688B2