HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647423Generated: October 30, 2026
Potassium Hydroxide → HCID 20484902, compound
https://huagongshe.com/reaction/647423
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 20484886 | HCID 20484886 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20484902 | HCID 20484902 | 14.5% |
Reaction Steps
Ethyl 2-{4-[N-(1-chloroisoquinolin-3-yl)-N-methylamino]phenoxy}propionate (2.87 g), in a solution of potassium hydroxide (0.42 g) in ethanol, was hydrogenated at atmospheric pressure over a palladium on carbon catalyst. After uptake of the theoretical amount of hydrogen the solution was filtered to remove the catalyst and the solvent was removed by distillation under reduced pressure. The product was purified by column chromatography over silical gel (eluant dichloromethane/ethylacetate; 99:1) to give ethyl 2-{4-[N-(isoquinolin-3-yl)-N-methylamino]phenoxy}propionate (0.38 g) as a green oil. The assigned structure was confirmed by proton magnetic resonance spectroscopy and mass spectrometry. Proton magnetic resonance spectrum (CDCl3 ; δ in ppm): 1.20 (3H, t); 1.60 (3H, d); 3.45 (3H, s); 4.20 (2H, q); 4.70 (1H, q); 6.60 (1H, s); 6.8-7.4 (7H, m); 7.65 (1H, d); 8.90 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04409017 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-d60d74c0cf0a46f19d97eb206136ce86 |
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| Source note | uspto-grants-1983_10 |
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