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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489749Generated: October 26, 2026

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

https://huagongshe.com/reaction/489749

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 numberUS06979695B2
Source datasetuspto-grants-2005_12
ORD IDord-76346d505f3440df9ce52fd40d74b013
Source noteuspto-grants-2005_12