HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449847Generated: October 26, 2026
Methanol → (3-Allyloxy-pyridin-2-yl)-methanol
https://huagongshe.com/reaction/449847
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 3-Hydroxy-2-(hydroxymethyl)pyridine hydrochloride | HCID 3084185 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Water | HCID 962 | — |
| Product | (3-Allyloxy-pyridin-2-yl)-methanol | HCID 14598977 | 62% |
Reaction Steps
Hydroxy-2-(hydroxymethyl)pyridine hydrochloride (50 g, 339.6 mmol) and methanol (250 mL) are combined under nitrogen and cooled to 22° C. To the vigorously stirred mixture is added 4.5 M sodium methoxide in MeOH (170.8 mL, 747.2 mmol). The mixture is stirred at room temperature for 2 h and then the solvent is evaporated. The resulting material is dissolved in DMSO (250 mL), allyl bromide (41 g, 339.6 mmoles) is added, and the mixture stirred for 18 h at room temperature. The reaction mixture is added to water (800 mL) and extracted with methylene chloride (3×80 mL). The organic portions are combined and dried over sodium sulfate, filtered, and the solvent evaporated to afford the title compound (34.4 g, 62%). LC-ES/MS m/z 166.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486943B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-3c0e8652eb3f4c2bafbc23a74e5f7fc7 |
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| Source note | uspto-grants-2013_07 |
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