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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278943Generated: October 27, 2026

Methyl iodide → N,N-dibenzyl-2-(1-methoxycyclopropyl)ethanamine

https://huagongshe.com/reaction/2278943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1-[2-(Dibenzylamino)ethyl]cyclopropanolHCID 57457828—
SolventTetrahydrofuranHCID 8028—
ProductN,N-dibenzyl-2-(1-methoxycyclopropyl)ethanamineHCID 8981452538.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 0° C. solution of 1-(2-(dibenzylamino)ethyl)cyclopropanol (3 g, 10.6 mmol) in THF (50 mL), under N2, was treated portion-wise with NaH (60%, 0.85 g, 21.3 mmol), stirred at 0° C. for 0.5 h, treated drop-wise with MeI (1.82 g, 12.8 mmol), warmed to RT and stirred for 3 h. The mixture was cooled to 0° C., quenched with satd. NH4Cl and partially concentrated. The residue was extracted with EtOAc (3×) and the combined organics were washed with brine, dried over Na2SO4, concentrated and purified via silica gel chromatography to afford N,N-dibenzyl-2-(1-methoxycyclopropyl)ethanamine (1.2 g, 38%). 1H NMR (400 MHz, CDCl3): δ 7.39-7.21 (m, 10 H), 3.60 (s, 4 H), 3.12 (s, 3 H), 2.65 (t, J=8 Hz, 2 H), 1.75 (t, J=8 Hz, 2 H), 0.68-0.65 (m, 2 H), 0.34-0.31 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133183B2
Source datasetuspto-grants-2015_09
ORD IDord-859d322bca53416e81367c6383f6823a
Source noteuspto-grants-2015_09