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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395076Generated: October 29, 2026

Methanol → Methyl 4-[3-(3-benzyloxy-2-pyridyl)prop-2-enyl]benzoate

https://huagongshe.com/reaction/2395076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant4-[3-(3-Benzyloxy-2-pyridyl)prop-2-enyl)benzoic acidHCID 54449459—
ProductMethyl 4-[3-(3-benzyloxy-2-pyridyl)prop-2-enyl]benzoateHCID 5450874949%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-[3-(3-Benzyloxy-2-pyridyl)prop-2-enyl)benzoic acid (0.1 g, 0.29 mmol) was dissolved in methanol (5 ml) and cooled to 0° C. To the solution was added thionyl chloride (0.086 g, 0.73 mmol). The reaction was allowed to warm to ambient temperature and stirred at ambient temperature for 18 hours. The reaction mixture was then evaporated, the residue partitioned between ethyl acetate and water and the organic phase dried (MgSO4) and evaporated. The residue was purified by chromatography (SiO2 EtOAc/CH2Cl2) to give methyl 4-[3-(3-benzyloxy-2-pyridyl)prop-2-enyl]benzoate as an oil (0.05 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811459
Source datasetuspto-grants-1998_09
ORD IDord-0999835e5f0d44ac90f78734e89367ce
Source noteuspto-grants-1998_09