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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 32867Erstellt: 24. Oktober 2026

Potassium Iodide → Phenylalanine,N-acetyl--phenyl-

https://huagongshe.com/de/reaction/32867

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktAcetamidomalonic acid diethyl esterHCID 14041—
EduktSodium HydroxideHCID 14798—
EduktDichlorodiphenylmethaneHCID 16327—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktPhenylalanine,N-acetyl--phenyl-HCID 1102240083,7%

Reaktionsschritte

To a solution (1.25 M) of diethyl acetamidomalonate (13.33 g, 61.8 mmol) in N-methyl-2-pyrrolidone (40 mL) was added potassium t-butoxide (7.20 g, 64.3 mmol), and the mixture was stirred at room temperature for 1 hr. Diphenylmethylene chloride (10.0 g, 49.3 mmol) and potassium iodide (4.10 g, 24.7 mol) were added, and the mixture was stirred at 70° C. for 6 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 60° C. for 5 hrs. The reaction mixture was allowed to cool to room temperature and the mixture was partitioned. The aqueous layer was adjusted to pH 7.0 with concentrated hydrochloric acid (4.4 mL). Ethyl acetate (80 mL) was added, and then concentrated hydrochloric acid (6.9 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 (20 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 (11.69 g). The powder X-ray (Cu—Kα ray) of the dry crystals showed characteristic peaks at 5.8°, 11.5°, 21.6°, 23.2° and 28.7°, as shown in FIG. 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07427688B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-98e9ee42f8224343ab261c98a0f92a4e
Quellennotizuspto-grants-2008_09