HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927581Generated: October 25, 2026
3-Oxetanone → 6-Cyclopropylmethoxy-5-(3-hydroxy-oxetan-3-yl)-pyridine-2-carboxylic acid
https://huagongshe.com/reaction/927581
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Reactant | 5-Bromo-6-cyclopropylmethoxy-pyridine-2-carboxylic acid | HCID 71087543 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Cyclopropylmethoxy-5-(3-hydroxy-oxetan-3-yl)-pyridine-2-carboxylic acid | HCID 71087650 | 30.8% |
Reaction Steps
Under a nitrogen atmosphere, n-BuLi (3.23 mL, 5.6 mmol) was added dropwise to a solution of 5-bromo-6-cyclopropylmethoxy-pyridine-2-carboxylic acid (Example 9 d, 1.1 g, 4.0 mmol) in THF (50 mL) at −78° C. and stirred for 1 h at this temperature. Then a solution of oxetan-3-one (CAN 6704-31-0, 0.73 g, 10 mmol) in THF (5 mL) was added at −78° C. The reaction mixture was stirred for 1 h at room temperature and quenched with aq. NH4Cl solution. The pH was adjusted to 2 with conc. HCl. The mixture was extracted with ethyl acetate (3×50 mL), the organic layers were combined, washed with brine (2×50 mL) and dried over Na2SO4. The solvent was removed under reduced pressure and the crude product was purified by chromatography over silica gel using petroleum ether/ethyl acetate=1/1 to give the title compound (0.13 g, 30.8%) as a yellow solid; MS (EI): m/e=266.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290451B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-edc2b492a33a4aaf977bb99f5c7fcf69 |
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| Source note | uspto-grants-2016_03 |
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