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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374535Erstellt: 25. Oktober 2026

Benzyl chloroformate → 2-{[(Benzyloxy)carbonyl]amino}-3-(thiophen-2-yl)propanoic acid

https://huagongshe.com/reaction/374535

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl chloroformateHCID 10387—
EduktPotassium CarbonateHCID 11430—
Edukt2-ThienylalanineHCID 91444—
EduktEtOAc AcOH CH3CN H2OHCID 131719237—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-{[(Benzyloxy)carbonyl]amino}-3-(thiophen-2-yl)propanoic acidHCID 1280683098%

Reaktionsschritte

To a mixture of 3.0 g (16.9 mmol) of β-thienyl-D,L-alanine in 75 mL of water and 60 mL of dioxane, was added 5.6 g (40.6 mmol) of anhydrous potassium carbonate, followed by 2.85 mL (20 mmol) of carbobenzyloxychloride. The resulting mixture was stirred rapidly for approximately one hour. When the reaction was substantially complete, as indicated by thin layer chromatography (21/7/7/9, ethyl acetate/acetic acid/acetonitrile/water), the reaction mixture was concentrated. The resultant layers were separated and the aqueous layer was washed with 75 mL of diethyl ether and then layered with 150 mL of methylene chloride. The resultant mixture was acidified with rapid stirring to pH=2.0 using 5N hydrochloric acid. The layers were then separated, and the organic layer was dried sodium sulfate (Na2SO4), filtered and concentrated to provide 5.05 g of desired compound (98%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05480887
Quelldatensatzuspto-grants-1996_01
ORD IDord-c7f3fc7a4e744d51ba5908cef44464ab
Quellennotizuspto-grants-1996_01