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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975674Generated: October 25, 2026

4-Pyridinecarboxaldehyde → 3-Pyridin-4-YL-acrylic acid methyl ester

https://huagongshe.com/reaction/1975674

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
SolventTetrahydrofuranHCID 8028—
Product3-Pyridin-4-YL-acrylic acid methyl esterHCID 98163—

Reaction Steps

Methyl (triphenylphosphoranylidene)acetate (3.4 grams) and 4-pyridine-carboxaldehyde (10.00 grams) were refluxed in tetrahydrofuran under nitrogen overnight. The reaction was evaporated in vacuo, and the residue was suspended in hexane (400 mi), heated to boiling on a steam bath for 5 minutes, and filtered through a filter aide. The filter cake was rinsed with hot hexane (2×200 mL), and the rinses and filtrate were combined and evaporated in vacuo. The crude product was purified by flash chromatography through silica gel 60 (1500 mi) using 3:7 ethyl acetate:methylene chloride. The resulting waxy solid was suspended in a minimum amount of cyclohexane to yield the product as a white crystalline solid. Yield: 7.06 grams (46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288719
Source datasetuspto-grants-1994_02
ORD IDord-c65e6b9c55144c25b6498e8251701bd5
Source noteuspto-grants-1994_02