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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1726755Erstellt: 26. Oktober 2026

Hydrochloric Acid → 3-(9H-fluoren-9-ylmethoxycarbonylamino)cyclohexane-1-carboxylic Acid

https://huagongshe.com/reaction/1726755

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
EduktSodium BicarbonateHCID 516892—
Edukt3-Aminocyclohexanecarboxylic acidHCID 544887—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(9H-fluoren-9-ylmethoxycarbonylamino)cyclohexane-1-carboxylic AcidHCID 426011057%

Reaktionsschritte

3-Aminocyclohexanecarboxylic acid (10 g, 70 mmol) was added to a solution of sodium hydrogen carbonate (7.6 g, 91 mmol) in water (100 mL). A solution of 1-[[(9H-fluoren-9-ylmethoxy)carbonyl]oxy-2,5-pyrrolidinedione (Fmoc-OSu; 28.3 g, 84 mmol) in tetrahydrofuran (200 mL) was added. The solution was stirred at room temperature overnight and then poured into 3 M HCl (200 mL). The mixture was extracted with ethyl acetate (100 mL then 50 mL) and the combined organic layers were washed with saturated brine (3×100 mL), dried (Na2SO4), filtered, and concentrated to approximately 200 mL. Crystallization occurred on concentration. The mixture was allowed to stand overnight, then the solid was filtered off, washed with ethyl acetate and dried in a vacuum oven at 55° C. to give 3-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]amino]cyclohexanecarboxylic acid (14.66, 57%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07491741B2
Quelldatensatzuspto-grants-2009_02
ORD IDord-718bb9127cbe44738f9bef647d73933e
Quellennotizuspto-grants-2009_02