HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350014Generated: October 25, 2026
m-Chloroperbenzoic acid → 5-Phenyl-2-pyridylmethyl acetate
https://huagongshe.com/reaction/350014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Methyl-5-phenylpyridine | HCID 76744 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Phenyl-2-pyridylmethyl acetate | HCID 23025060 | 92% |
Reaction Steps
A mixture of 2-methyl-5-phenylpyridine (3.00 g), 3-chloroperbenzoic acid (4.79 g) and tetrahydrofuran (50 ml) was stirred at room temperature overnight, and concentrated. The residue was subjected to silica gel column chromatography to obtain a colorless oily substance from the fraction eluted with tetrahydrofuran. A solution of the resulting colorless oily substance in acetic anhydride (50 ml) was added slowly to acetic anhydride (50 ml) heated at 130° C., which was stirred at 2 hours, and concentrated. The residue was dissolved in ethyl acetate, which was washed with saturated aqueous sodium bicarbonate solution, and with saturated aqueous sodium chloride solution, and then dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography to obtain 5-phenyl-2-pyridylmethyl acetate (3.68 g, yield 92%) as colorless crystals from the fraction eluted with ethyl acetate-hexane (1:2, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 71–72° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07179823B1 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-695e36304ce24f708b060f7f3d7bafad |
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| Source note | uspto-grants-2007_02 |
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