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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49600Generated: October 24, 2026

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

https://huagongshe.com/en/reaction/49600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-(3-Hydroxy-1-azabicyclo[2.2.2]oct-3-yl)acetic acid t-butyl esterHCID 45357691—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-{3-hydroxy-1-azabicyclo[2.2.2]octan-3-yl}acetateHCID 2186226748.6%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706878B2
Source datasetuspto-grants-2004_03
ORD IDord-9ca5c103a2034145b1928055e9726dba
Source noteuspto-grants-2004_03