HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463325Generated: October 27, 2026
Triethylene Glycol → 4-(4-Ethylphenoxy)piperidine
https://huagongshe.com/reaction/463325
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylene Glycol | HCID 8172 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Oxalate | HCID 71081 | — |
| Reactant | 1-{4-[(Piperidin-4-yl)oxy]phenyl}ethan-1-one | HCID 13457427 | — |
| Product | 4-(4-Ethylphenoxy)piperidine | HCID 13457429 | 38.6% |
Reaction Steps
A solution of 4-(4-acetylphenoxy)piperidine (liberated from 15.0 g, 48.5 mmol, of the oxalate), 7.45 g of potassium hydroxide, 5.39 ml of 85% hydrazine hydrate and 54 ml of triethyleneglycol was stirred at reflux for 1 hour. The mixture was then cooled to room temperature and the flask fitted with a distillation apparatus. The temperature was then raised to 190°-195° and water removed by distillation. The mixture was stirred at 190°-195° for 3 hours and the mixture allowed to cool to room temperature. The mixture was diluted with water, extracted twice with ether and with 1N HCl, made basic with saturated sodium carbonate, extracted with ether and dried over potassium carbonate. Filtration followed by evaporation of the solvent provided an oil. Kugelrohr distillation at 114°-116°/1 mm provided 3.84 g (18.7 mmol, 38.6%) of 4-(4-ethylphenoxy)piperidine, m.p. 37-41.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04518713 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-252253e7c675432f96f0686e96717777 |
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| Source note | uspto-grants-1985_05 |
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