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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977138Generated: November 1, 2026

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

https://huagongshe.com/reaction/1977138

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 numberUS06232316B1
Source datasetuspto-grants-2001_05
ORD IDord-f96a41b7ccd84bdab3d773550c7fcf56
Source noteuspto-grants-2001_05