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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62620Generated: October 30, 2026

Methyl iodide → 3-(Methylamino)bicyclo[1.1.1]pentan-1-yl acetate

https://huagongshe.com/reaction/62620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Aminobicyclo[1.1.1]pentan-1-yl acetateHCID 90411187—
SolventDimethylformamideHCID 6228—
Product3-(Methylamino)bicyclo[1.1.1]pentan-1-yl acetateHCID 90410974—

Reaction Steps

To an anhydrous DMF (5 mL) solution of 3-aminobicyclo[1.1.1]pentan-1-yl acetate (1 mmol; prepared as described in Example 1, Step 2) is added potassium carbonate (3 mmol) followed by the addition of methyl iodide (1 mmol) by syringe at r.t. The reaction is monitored by LCMS and TLC. After consumption of starting material, the reaction mixture is quenched by adding water (3 mL) and extracted with ethyl acetate (3×). The organic layers are combined, dried (magnesium sulfate), filtered, and concentrated. The crude residue is subjected to flash chromatography (silica gel, EtOAc/hexanes) to afford 3-(methylamino)bicyclo[1.1.1]pentan-1-yl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447026B2
Source datasetuspto-grants-2016_09
ORD IDord-697c0bc3bb00499ba6e5397202f3723d
Source noteuspto-grants-2016_09