HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906468Generated: November 1, 2026
Dimethyl Sulfoxide → 3-(Benzyloxy)-2-chloropyridine
https://huagongshe.com/reaction/1906468
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | 2-Chloro-3-pyridinol | HCID 81136 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Benzyloxy)-2-chloropyridine | HCID 819374 | — |
Reaction Steps
2-Chloro-3-hydroxypyridine (9.47 g; 0.073 moles) was added to a solution of sodium ethoxide in ethanol (from sodium, 1.67 g; 0.073 g. atom). Sufficient dimethyl sulphoxide was added to dissolve all of the solid, and ethanol was removed in vacuo . To the resulting solution was added benzyl chloride (9.3 g; 0.073 moles) with cooling and stirring, and the reaction mixture was left to stir under reflux for 6 hours. Unreacted benzyl chloride, and solvent, were evaporated off under vacuum on a boiling water bath, and the residue was treated with water to precipitate out an oil which was extracted with chloroform, washed with N sodium hydroxide solution and dried over anhydrous magnesium sulfate. After removing the solvent, 2-chloro-3-benzyloxypyridine was obtained as a solid (11.63 g, mp 36°-8°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04652572 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-1233be504a454cf696bd91ee052413cb |
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| Source note | uspto-grants-1987_03 |
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