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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828921Generated: October 29, 2026

Methylamine → 4-Penten-2-amine, N-methyl-5-(3-pyridinyl)-, (2S,4E)-

https://huagongshe.com/reaction/1828921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant(2R)-(4E)-5-(3-Pyridyl)4-penten-2-ol p-ToluenesulfonateHCID 87466997—
SolventEthanolHCID 702—
Product4-Penten-2-amine, N-methyl-5-(3-pyridinyl)-, (2S,4E)-HCID 983410724%

Reaction Steps

A mixture of (2R)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonate (9.00 g, 28.35 mmol), methylamine (200 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 1.20 g (24.0%) of a colorless oil, bp 90–100° C. at 0.5 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060826B2
Source datasetuspto-grants-2006_06
ORD IDord-f731ba48cbee48f2ac4e1b0ba3f8c3ad
Source noteuspto-grants-2006_06