HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 466342Erstellt: 24. Oktober 2026
Hydrochloric Acid → 1,3-Bis(2,2-dimethyl-4-pentenoyloxy)-propane
https://huagongshe.com/de/reaction/466342
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 1,3-Dibromopropane | HCID 8001 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2,2-Dimethyl-4-pentenoic acid | HCID 140065 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1,3-Bis(2,2-dimethyl-4-pentenoyloxy)-propane | HCID 19745526 | 68,5% |
Reaktionsschritte
To a mixture of 2.6 g (0.02 mole) of 2,2-dimethyl-4-pentenoic acid (XII) and 50 ml of hexamethylphosporic triamide a solution of 1.2 g (0.03 mole) of sodium hydroxide in 3.6 ml of water is added. The reaction mixture is stirred at room temperature for 1 hour and then 1.2 ml (2.4 g, 0.012 mole) of 1,3-dibromopropane are added. The mixture is stirred at room temperature for 4 hours, then poured onto 100 ml of 5% aqueous hydrochloric acid and extracted twice with 50 ml of diethyl ether each. The organic phase is washed twice with 25 ml of water each, dried over sodium sulfate and the solvent is distilled off under reduced pressure. The crude product thus obtained is purified by chromatography on a silica gel column eluted with a 7:3 mixture of hexane and diethyl ether. Thus 2.03 g of the desired compound are obtained in the form of a colourless oil. Yield: 68.5%. According to TLC chromatography using the above-specified eluent Rf =0.6.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05155260 |
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| Quelldatensatz | uspto-grants-1992_10 |
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| ORD ID | ord-d0e06574e7ca4cc7951fc21f74d5cc03 |
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| Quellennotiz | uspto-grants-1992_10 |
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