HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834514Generated: October 31, 2026
4-Methoxy-4-(1-methylethyl)piperidine → HCID 20373715, compound
https://huagongshe.com/reaction/1834514
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxy-4-(1-methylethyl)piperidine | HCID 20373713 | — |
| Reactant | HCID 54135253 | HCID 54135253 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20373715 | HCID 20373715 | — |
Reaction Steps
To a mixture of 21.5 g (0.1 m) of gamma-(p-fluorophenyl)-gamma-oxo-butyric acid chloride and 15.7 (0.1 m) of 4-isopropyl-4-methoxy-piperidine in 200 ml of benzene, 15.5 ml (0.11 m) of triethylamine is added. The triethylamine hydrochloride formed is filtered off and the solvent removed by evaporation under vacuum on a steambath. The residue is dissolved in dry ether and added dropwise to a suspension of 15 g of lithium aluminum hydride in ether. The reaction mixture is refluxed for two hours and the obtained mixture decomposed with water. The precipitate is filtered off and the ether solution evaporated. The residue, which consists of the alcohol corresponding to the butyrophenone, is oxidized according to Oppenauer with 60 g of aluminum-isopropylate in 500 ml of dry acetone. The reaction mixture is refluxed for 12 hours, cooled, and decomposed with water. After centrifugation, the solution is evaporated to dryness, whereafter the residue dissolved in ether and the hydrochloride precipitated with alcoholic hydrochloric acid. After recrystallization, the hydrochloride melts at 190°-192° C. Yield 19 g. The tartrate is prepared using tartaric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04070473 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-9e005c157001412d82387cf87c3c949c |
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| Source note | uspto-grants-1978_01 |
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