HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222287Generated: October 27, 2026
Water → Ethyl 2-(6-quinolinyloxy)-2-(ethoxy)acetate
https://huagongshe.com/reaction/2222287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 6-Hydroxyquinoline | HCID 11374 | — |
| Reactant | Ethyl 2-chloro-2-ethoxyacetate | HCID 2724873 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | Ethyl 2-(6-quinolinyloxy)-2-(ethoxy)acetate | HCID 21923123 | 64.7% |
Reaction Steps
Potassium t-butoxide (3.15 g) was dissolved in t-butyl alcohol (20 ml) and stirred for 10 minutes at ambient temperature. 6-Hydroxyquinoline (3.0 g) was added, the resulting dark green solution was stirred for 15 minutes, and then ethyl 2-chloro-2-ethoxyacetate (4.22 g, 90% pure) added, followed by a catalytic amount of potassium iodide (0.005 g). The mixture was stirred for 18 hours, poured into water and extracted with chloroform. The organic fraction was washed with brine, water, and dried over magnesium sulphate. The solvent was evaporated to give a brown oil, which was purified by flash chromatography on silica gel, eluting with a gradient of ethyl acetate:hexane (1:2 to 4:1) to give ethyl 2-(6-quinolinyloxy)-2-(ethoxy)acetate as a pale brown oil (3.68 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371764B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-49a524784f154afebfe512bc0c7a7d73 |
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| Source note | uspto-grants-2008_05 |
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