HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869905Generated: October 30, 2026
Potassium Carbonate → 4-bromo-1-(2-hydroxyethyl)pyridin-2(1H)-one
https://huagongshe.com/reaction/869905
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Iodoethanol | HCID 12225 | — |
| Reactant | 4-Bromo-2-hydroxypyridine | HCID 817115 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-bromo-1-(2-hydroxyethyl)pyridin-2(1H)-one | HCID 68738532 | 13.8% |
Reaction Steps
To a solution of 4-bromopyridin-2(1H)-one (174 mg, 1.00 mmol) in THF (3.5 mL) was added K2CO3 (1.38 g, 10.0 mmol) and 2-iodoethanol (156 μL, 2.00 mmol). The reaction was stirred at 80° C. for 2 days before being cooled to room temperature and filtered. The filtrate was concentrated and purified by column chromatography (0-10% MeOH—CH2Cl2) to yield 4-bromo-1-(2-hydroxyethyl)pyridin-2(1H)-one as a pale yellow solid (30 mg, 7%). ESI-MS m/z calc. 217.0. found 218.3 (M+1)+. Retention time 0.33 minutes. 1H NMR (400 MHz, DMSO-d6) δ 7.57 (d, J=7.2 Hz, 1H), 6.70 (d, J=2.2 Hz, 1H), 6.44 (dd, J=2.2, 7.2 Hz, 1H), 4.89 (t, J=5.4 Hz, 1H), 3.91 (t, J=5.4 Hz, 2H), 3.59 (q, J=5.4 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969386B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-35ef8e46d9514ff6ba086e7a576277ca |
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| Source note | uspto-grants-2015_03 |
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