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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48503Erstellt: 24. Oktober 2026

Trifluoroacetic acid → Methyl 2-{3-hydroxy-1-azabicyclo[2.2.2]octan-3-yl}acetate

https://huagongshe.com/de/reaction/48503

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
Edukt2-(3-Hydroxy-1-azabicyclo[2.2.2]oct-3-yl)acetic acid t-butyl esterHCID 45357691—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 2-{3-hydroxy-1-azabicyclo[2.2.2]octan-3-yl}acetateHCID 2186226748,6%

Reaktionsschritte

Trifluoroacetic acid (40 mL) was added dropwise over 15 minutes to a solution of 2-(3-hydroxy-1-azabicyclo[2.2.2]oct-3-yl)acetic acid t-butyl ester (15.7 g) in anhydrous dichloromethane (40 mL) at 0° C. The mixture was stirred for 24 hours at room temperature, then the solvent was evaporated under reduced pressure. The residue was dissolved in methanol (90 mL) and cooled in an ice bath. Concentrated sulfuric acid (9 mL) was added dropwise over 10 minutes, then the reaction mixture was stirred at room temperature. After 3 hours, the solution was poured into 100 mL of ice water, basified to pH 10 with saturated aqueous sodium carbonate solution, and extracted with chloroform (4×100 mL). The extracts were dried (MgSO4), filtered, and evaporated in vacuo to give a solid. Recrystallization from ethyl acetate provided 6.3 g of the tan crystalline subtitle compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06703502B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-bec9c82dfbf84a6c8212e47e29156169
Quellennotizuspto-grants-2004_03