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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824738Generated: November 2, 2026

Methylamine → (4E)-N-Methyl-5-(3-pyridyl)-4-penten-2-amine

https://huagongshe.com/reaction/1824738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant(4E)-5-(3-Pyridyl)-4-pentene-2-ol p-ToluenesulfonateHCID 87466987—
SolventEthanolHCID 702—
Product(4E)-N-Methyl-5-(3-pyridyl)-4-penten-2-amineHCID 1021965451.6%

Reaction Steps

A mixture of (4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonate (5.60 g, 17.66 mmol), methylamine (100 mL, 40% solution in water), and ethyl alcohol (10 mL) was stirred at ambient temperature for 18 h. The resulting solution was extracted with chloroform (3×100 mL). The combined chloroform extracts were dried over sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was purified by column chromatography over aluminum oxide, eluting with ethyl acetate-methanol (7:3, v/v). Selected fractions were combined and concentrated by rotary evaporation, producing an oil. Further purification by vacuum distillation furnished 1.60 g (51.6%) of a colorless oil, bp 110–120° C. at 0.1 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045538B2
Source datasetuspto-grants-2006_05
ORD IDord-e7228faeacef44aca4d0eb476531def2
Source noteuspto-grants-2006_05