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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1600525Erstellt: 24. Oktober 2026

Hydrochloric Acid → Boc-homophenylalaninal

https://huagongshe.com/reaction/1600525

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-MethylmorpholineHCID 7972—
EduktIsobutyl chloroformateHCID 62365—
EduktCP 84364HCID 664657—
Eduktethyl (S)-4-amino-6-phenyl-2-hexenoate hydrochlorideHCID 86754733—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBoc-homophenylalaninalHCID 1026474080%

Reaktionsschritte

Morpholinecarbonylphenylalanine (2.74 g, 9.82 mmol, prepared according to the method described in Esser, R. et.al., Arthritis & Rheumatism (1994), 0000) was dissolved in THF (50 mL) at -10° C. 4-methylmorpholine (1.08 mL, 9.82 mmol) was added, followed by isobutyl chloroformate (1.27 mL, 9.82 mmol). The mixed anhydride was stirred for 10 minutes, whereupon a solution of ethyl (S)-4-amino-6-phenyl-2-hexenoate hydrochloride from the previous step in DMF (10 mL) was added, followed by 4-methylmorpholine (1.08 mL, 9.82 mmol). The mixture was stirred for 1 hour. 1M HCl (50 mL) was added. The product was extracted with ethyl acetate (100 mL), washed with saturated aqueous NaHCO3 (50 mL), dried over MgSO4 and decolorizing charcoal (DARCO), filtered, and evaporated to dryness, giving 3.80 g (80% yield from Boc-homophenylalaninal).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05976858
Quelldatensatzuspto-grants-1999_11
ORD IDord-acf3b734ba6c4d49893738d6d94827e3
Quellennotizuspto-grants-1999_11