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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62615Generated: November 1, 2026

Ethyl Acetate → 1-{3-Aminobicyclo[1.1.1]pentan-1-yl}ethan-1-one

https://huagongshe.com/reaction/62615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Aminobicyclo(1.1.1)pentane-1-carboxylic acidHCID 25324661—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
Product1-{3-Aminobicyclo[1.1.1]pentan-1-yl}ethan-1-oneHCID 90410811—

Reaction Steps

To a solution of 3-aminobicyclo[1.1.1]pentane-1-carboxylic acid (1 mmol) in anhydrous THF (2 mL) at 0° C. under nitrogen is added a methyllithium (1.4 M in diethyl ether, 4 mmol) in a dropwise manner. After addition, the reaction mixture is slowly allowed to warm to room temperature (r.t.), stirred overnight, and treated with aqueous saturated ammonium chloride solution (4 mL). Ethyl acetate (2 mL) is added and organic layer are separated. The aqueous layer is extracted with ethyl acetate (3×1 mL). The combined organic layers are dried (Mg2SO4) and concentrated. The residue is purified by a flash chromatography on silica gel (EtOAc/hexanes) to give 1-(3-aminobicyclo[1.1.1]pentan-1-yl)ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447026B2
Source datasetuspto-grants-2016_09
ORD IDord-2a6f5e3f0b0442759f3fd669807d73a4
Source noteuspto-grants-2016_09