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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837269Generated: November 3, 2026

Methylamine → 3-(benzyloxy)-N-methylpropan-1-amine

https://huagongshe.com/reaction/1837269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantBenzyl 3-Bromopropyl EtherHCID 2776064—
SolventTetrahydrofuranHCID 8028—
Product3-(benzyloxy)-N-methylpropan-1-amineHCID 23497039—

Reaction Steps

3.57 g of methylamine is condensed in a solution of 1.8 ml of (3-bromo-propoxymethyl)-benzene in 15 ml of anhydrous tetrahydrofuran at −78° C., and it is stirred overnight at room temperature in a pressurized reactor. After the pressurized reactor was opened at −20° C., it is allowed to come to room temperature to allow excess methylamine to evaporate off. Then, the reaction solution is added to saturated sodium chloride solution, extracted with ether, dried on magnesium sulfate and concentrated by evaporation in a vacuum. 1.91 g of (3-benzyloxy-propyl)-methyl-amine is obtained as a crude product, which is used without further purification in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780855B2
Source datasetuspto-grants-2004_08
ORD IDord-0fbd7af9fbb546fe9f252085efa052d8
Source noteuspto-grants-2004_08