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HRID 4316Erstellt: 23. Oktober 2026
Dichloromethane → 1,3-Bis[4-(4-chlorobenzyl)-1-piperazinyl]-1,3-dioxopropane dihydrochloride monohydrate
https://huagongshe.com/de/reaction/4316
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Propanedioyl dichloride | HCID 74269 | — |
| Edukt | 4-Chlorobenzylpiperazine | HCID 134826 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 1,3-Bis[4-(4-chlorobenzyl)-1-piperazinyl]-1,3-dioxopropane dihydrochloride monohydrate | HCID 20152227 | 45,1% |
Reaktionsschritte
A mixture of 4.2 g of 1-(4-chlorobenzyl)piperazine, 1.4 g of malonyl dichloride, 10 g of methylene chloride and 2.0 g of triethylamine was stirred for 60 hours. The reaction mixture was made basic with 2N sodium hydroxide. The organic layer was separated, and the aqueous phase was extracted with three 50 ml portions of ether, followed by three 50 ml portions of methylene chloride. The organic phases were combined and mixed with 100 ml of 2N hydrochloric acid. The aqueous phase was separated and made basic with 2N sodium hydroxide solution. The resulting oil was collected and chromatographed on silica, the eluant being CH2Cl2 /CH2OH/ammonium hydroxide (200:5:1). The appropriate fractions were combined, evaporated to an oil, dissolved in 100 ml of ether and precipitated with excess anhydrous hydrogen chloride. The precipitate was recrystallized from reagent ethanol to yield 1.3 g (22% of theory) of 1,3-bis[4-(4 -chlorobenzyl)-1-piperazinyl]-1,3-dioxopropane dihydrochloride monohydrate as a very slightly yellow crystalline solid (m.p. 199°-206° C.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04725597 |
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| Quelldatensatz | uspto-grants-1988_02 |
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| ORD ID | ord-5fbf8b934342464383a21037ee00b589 |
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| Quellennotiz | uspto-grants-1988_02 |
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