HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767418Generated: October 31, 2026
Ethyl bromoacetate → [(Quinolin-4-yl)oxy]acetic acid
https://huagongshe.com/reaction/1767418
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | quinolin-4-ol | HCID 178516385 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | [(Quinolin-4-yl)oxy]acetic acid | HCID 22633686 | 29.5% |
Reaction Steps
The mixture of 4-hydroxyquinoline (290 mg, 2.0 mmol), potassium carbonate (910 mg, 6.6 mmol), ethyl bromoacetate (500 mg, 3.0 mmol) and acetone (25 ml) was refluxed for 8 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). Water layer was placed in cold room, and solid came out. The crystals were filtered with suction and washed with water, and then dried to give 120 mg quinoline-4-oxyacetic acid as gray crystals, mp 274-276° 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-1580b63e98db44aea6e2f127bcb02373 |
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| Source note | uspto-grants-2007_06 |
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