HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767415Generated: October 30, 2026
Ethyl bromoacetate → HCID 18317825, compound
https://huagongshe.com/reaction/1767415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Iodo-6-methylpyridin-3-ol | HCID 89957 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 18317825 | HCID 18317825 | 56.3% |
Reaction Steps
The mixture of 6-iodo-2-picolin-5-ol (235 mg, 1.0 mmol), potassium carbonate (455 mg, 3.3 mmol), ethyl bromoacetate (250 mg, 1.49 mmol) and acetone (15 ml) was refluxed for 15 h. After cooling, the mixture was filtered to remove potassium carbonate. The filtrate was concentrated under reduced pressure. To this residue, 10 ml dioxane and 14 ml 5% sodium hydroxide solution were added. After the mixture was stirred at room temperature overnight, it was acidified with concentrated hydrochloric acid to pH 3, and then extracted three times with ethyl acetate (20 ml each). Organic phases were combined, washed with water and brine, dried over magnesium sulfate, filtered, and then evaporated in vacuo. The residue was recrystallized from ethanol and petroleum ether to give 165 mg 6-iodo-2-methylpyridine-5-oxyacetic acid as white crystals, mp 170-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039707E1 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-73ef7ffe7fa4445888dcaced88d53c24 |
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| Source note | uspto-grants-2007_06 |
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