HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769262Generated: October 26, 2026
Triethylamine → 2-(Propargyloxy)ethyl 5-chloroquinolin-8-oxyacetate
https://huagongshe.com/reaction/1769262
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Propynoxyethanol | HCID 77596 | — |
| Reactant | Cloquintocet | HCID 15257197 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 2-(Propargyloxy)ethyl 5-chloroquinolin-8-oxyacetate | HCID 18947640 | 16.4% |
Reaction Steps
5.0 g (0.021 mol) of 5-chloroquinolin-8-oxyacetic acid are heated at 70° C. in 70 ml of thionyl chloride for one hour. The excess thionyl chloride is then distilled off in vacuo and the residue is suspended in 150 ml of carbon tetrachloride. 2.10 g (0.021 mol) of 2-propargyloxyethanol are added dropwise to this suspension, 2.30 g (0.023 mol) of triethylamine are then added dropwise and the mixture is heated under reflux for 12 hours. The suspension is then washed with in each case 70 ml of 2N HCl and 5 percent strength sodium hydroxide solution, the organic phase is dried over magnesium sulfate and the solvent is stripped off in vacuo. The residue is recrystallized from n-heptane. 1.1 g (16.3% of theory) of 2-(propargyloxy)ethyl 5-chloroquinolin-8-oxyacetate of melting point 53° C. are thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05380852 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-473df83f70ce4276a069e3d7dbb0dbdf |
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| Source note | uspto-grants-1995_01 |
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