Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62603Generated: October 30, 2026

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

https://huagongshe.com/reaction/62603

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, 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/hexnaes) to give 1-(3-aminobicyclo[1.1.1]pentan-1-yl)ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447025B2
Source datasetuspto-grants-2016_09
ORD IDord-d6d47c5580c947a994e003316c6043c0
Source noteuspto-grants-2016_09