HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349949Generated: October 29, 2026
Thionyl Chloride → 4-Chloromethyl-2-(5-methyl-2-phenyl-4-oxazolylmethoxy)pyridine
https://huagongshe.com/reaction/349949
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-4-pyridylmethanol | HCID 17861375 | — |
| Product | 4-Chloromethyl-2-(5-methyl-2-phenyl-4-oxazolylmethoxy)pyridine | HCID 17861304 | 54% |
Reaction Steps
A mixture of 2-(5-methyl-2-phenyl-4-oxazolylmethoxy)-4-pyridylmethanol (1.19 g) and thionyl chloride (4 ml) was stirred at room temperature for 1 hour. After the reaction mixture was concentrated, saturated aqueous sodium bicarbonate solution was added to the mixture, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and concentrated. The residue was subjected to silica gel column chromatography to obtain 4-chloromethyl-2-(5-methyl-2-phenyl-4-oxazolylmethoxy)pyridine (680 mg, yield 54%) as colorless crystals from the fraction eluted with ethyl acetate-hexane (1:3, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 104–105° 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-25059e32088b40fdb830d3eb898ddc18 |
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| Source note | uspto-grants-2007_02 |
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