HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368111Generated: October 31, 2026
Hydrogen Peroxide → 6-(Cyclopropylmethoxy)pyridin-3-ol
https://huagongshe.com/reaction/2368111
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trimethylborane | HCID 68979 | — |
| Reactant | 5-Bromo-2-(cyclopropylmethoxy)pyridine | HCID 21914279 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(Cyclopropylmethoxy)pyridin-3-ol | HCID 57517500 | — |
Reaction Steps
To a solution of 5-bromo-2-(cyclopropylmethoxy)pyridine (1.88 g) in THF (15 mL) was added 1.6M n-butyllithium-hexane solution (7.25 mL) at −78° C., and the mixture was stirred at the same temperature for 20 min. Trimethylborane (1.29 mL) was added to this solution, and the mixture was stirred at −78° C. for 30 min. The reaction mixture was heated to 0° C., aqueous hydrogen peroxide (30%, 5 mL) and 8M aqueous sodium hydroxide solution (1.55 mL) were added thereto, and the mixture was stirred for 15 min. Water was added to the reaction mixture, the mixture was extracted twice with ethyl acetate, and the combined organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (855 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703758B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-c9cf9ddf13bd4a3eb8bfdb78ba40a378 |
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| Source note | uspto-grants-2014_04 |
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