HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349962Generated: October 25, 2026
Thionyl Chloride → 5-(Chloromethyl)-2-phenylpyridine
https://huagongshe.com/reaction/349962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (6-Phenylpyridin-3-yl)methanol | HCID 22254216 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(Chloromethyl)-2-phenylpyridine | HCID 2763862 | 89% |
Reaction Steps
Thionyl chloride (10 ml) was slowly added to a solution of 6-phenyl-3-pyridylmethanol (11.60 g) in toluene (100 ml) at room temperature, which was stirred at 100° C. for 1 hour. After cooling, the reaction mixture was poured into saturated aqueous sodium bicarbonate solution, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4) and concentrated to obtain 5-chloromethyl-2-phenylpyridine (11.49 g, yield 89%) as colorless crystals. This was recrystallized from ethyl acetate-hexane. Melting point: 95–96° 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-0d4cbb3c57be402f9753ac6ddd4e16a2 |
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| Source note | uspto-grants-2007_02 |
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