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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944565Generated: October 27, 2026

trans N-benzyl-2-methoxy-N-[(2-methylcyclopropyl)methyl]ethanamine hydrochloride → trans (2-Methoxyethyl)[(2-methylcyclopropyl)methyl]amine hydrochloride

https://huagongshe.com/reaction/1944565

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttrans N-benzyl-2-methoxy-N-[(2-methylcyclopropyl)methyl]ethanamine hydrochlorideHCID 86616986—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Producttrans (2-Methoxyethyl)[(2-methylcyclopropyl)methyl]amine hydrochlorideHCID 86616985—

Reaction Steps

To a solution of trans N-benzyl-2-methoxy-N-[(2-methylcyclopropyl)methyl]ethanamine hydrochloride (16 g, 59.3 mmol) in EtOH (400 mL), degassed with Argon, was added Pd(OH)2 (830 mg, 20%), and the mixture was stirred under 1 atm H2, at room temperature for 4 h. The reaction mixture was purged with N2, filtered on celite, under N2, concentrated in vacuo, and dried under vacuum over P2O5 to give trans (2-methoxyethyl)[(2-methylcyclopropyl)methyl]amine hydrochloride as a white foam. 1H NMR (400 MHz, CDCl3) δ 9.46 (bs, 2H), 3.84 (t, J=5.1 Hz, 2H), 3.40 (s, 3H), 3.23 (bt, J=5.1 Hz, 2H), 3.08-2.88 (m, 2H), 1.09 (d, J=6.1 Hz, 3H), 1.02-0.91 (m, 1H), 0.86-0.78 (m, 1H), 0.65-0.57 (m, 1H), 0.50-0.42 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394837B2
Source datasetuspto-grants-2013_03
ORD IDord-1ad66e14bb2f4407b9f090686873b935
Source noteuspto-grants-2013_03