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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 376001Erstellt: 25. Oktober 2026

Hydrochloric Acid → N-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimide

https://huagongshe.com/reaction/376001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium ChlorideHCID 5234—
Edukt(Vinyl-2-ylidenetris(oxy))tris(trimethylsilane)HCID 553067—
Edukt3-phenyl-2(S)-phthalimidopropionyl chlorideHCID 10567197—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktN-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimideHCID 1026731978%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

A mixture of 134 g of 3-phenyl-2(S)-phthalimidopropionyl chloride and 269.7 g of tris(trimethylsilyloxy)ethylene was stirred at 95° C. for 5 hours. A further 54 g of tris(trimethylsilyloxy)ethylene were added and the mixture was stirred at 95° C. for a further 1.5 hours. The cooled reaction mixture was then treated with 435 ml of dioxan and 174 ml of 0.6N hydrochloric acid and the resulting mixture was heated to 85° C. for 30 minutes. The cooled mixture was saturated with sodium chloride and then. extracted with diethyl ether. The ethereal solution was washed with aqueous sodium bicarbonate solution and evaporated. The resulting pale yellow solid was crystallized from ethyl acetate/n-hexane to give 103 g of N-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimide as a white solid, MS: m/e 310 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05488115
Quelldatensatzuspto-grants-1996_01
ORD IDord-7c4cdd09a8c04351b4d31ff9acd4d54b
Quellennotizuspto-grants-1996_01