HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290467Generated: October 30, 2026
Potassium Carbonate → HCID 20232620, compound
https://huagongshe.com/reaction/2290467
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 616056 | HCID 616056 | — |
| Reactant | HCID 20232558 | HCID 20232558 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 20232620 | HCID 20232620 | — |
Reaction Steps
A mixture of 13.9 g. (50.2 mmole) p-toluenesulphonic acid (3,5-di-tert.-butyl-4-hydroxyphenethyl)ester, 18.4 g. (45.6 mmole) ethyl 4-[2-(piperazin-1-yl)-ethyl]-phenylacetate, 6.3 g. potassium carbonate and 300 ml. butan-2-one is heated for 8 hours while stirring at reflux temperature. For protection against oxidation, the reaction is carried out under an atmosphere of nitrogen. After cooling, the inorganic precipitate is filtered off with suction, the filtrate is evaporated and the evaporation residue is taken up in diethyl ether. From the ether solution, the hydrochloride is precipitated with hydrogen chloride-containing diethyl ether. After recrystallisation from ethanol, there are obtained 16.4 g. (62% of theory) of the desired compound as hydrochloride; m.p. 247°-250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04616086 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-1846c29fc1f34e7b9ed9d84f5ff3eb31 |
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| Source note | uspto-grants-1986_10 |
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