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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206547Generated: October 31, 2026

1-(1,4-dioxan-2-yl)-N-(4-methoxybenzyl)ethanamine → HCID 54499564, compound

https://huagongshe.com/reaction/2206547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1,4-dioxan-2-yl)-N-(4-methoxybenzyl)ethanamineHCID 89739160—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 54499564HCID 5449956496%

Reaction Steps

To a solution of 1-(1,4-dioxan-2-yl)ethanone (12 g, 92.2 mmol) in 1,2-dichloroethane (100 mL) was added (4-methoxyphenyl)methanamine (25 g, 184.4 mmol) at room temperature. The mixture was allowed to stir for 3 hours, and then sodium triacetoxyborohydride (39 g, 184.4 mmol) was added. The resulting mixture was allowed to stir for 48 hours at room temperature. The reaction mixture was quenched by adding water, extracted with dichloromethane (100 mL×3). The combined organic phase was dried by anhydrous sodium sulphate, and then filtered. The filtrate was concentrated and purified by column chromatograph on silica gel (elute: dichloromethane/methanol 100:1→50:1→20:1) to give 1-(1,4-dioxan-2-yl)-N-(4-methoxybenzyl)ethanamine (16.4 g, 71%) as a yellow solid. LCMS (M+H+) m z: calcd. 251.15. found 251.9. To a solution of 1-(1,4-dioxan-2-yl)-N-(4-methoxybenzyl)ethanamine (5 g, 19.9 mmol) in anhydrous methanol (100 mL) was added palladium 10% on carbon (240 mg, 2 mmol), then purged with hydrogen (30 psi), the mixture was allowed to stir overnight at room temperature. The reaction mixture was filtered, and the filtrate was concentrated to afford the title compound (2.5 g, 96%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-0d0cd262750948fead24ddb2dd3293d9
Source noteuspto-grants-2016_06