HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 340871Erstellt: 24. Oktober 2026
Potassium Iodide → 2,5-Dimethylhexane-2,5-diyl bis(2-hydroxyacetate) isophthaloyl chloride 5-acetoxy isophthaloyl chloride
https://huagongshe.com/de/reaction/340871
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Isophthaloyl chloride | HCID 7451 | — |
| Edukt | Dabco | HCID 9237 | — |
| Edukt | Butanediol | HCID 165788 | — |
| Edukt | 1,3-Benzenedicarbonyl dichloride, 5-(acetyloxy)- | HCID 10515530 | — |
| Edukt | 2,5-Dimethylhexane-2,5-diyl bis(2-hydroxyacetate) | HCID 58282118 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 2,5-Dimethylhexane-2,5-diyl bis(2-hydroxyacetate) isophthaloyl chloride 5-acetoxy isophthaloyl chloride | HCID 131732089 | — |
Reaktionsschritte
A solution of 2,5-dimethylhexane-2,5-diyl bis(2-hydroxyacetate) (69) (0.997 g, 3.8 mmol), isophthaloyl chloride (115) (0.406 g, 2.0 mmol), 5-acetoxy isophthaloyl chloride (117) (0.522 g, 2.0 mmol), a catalytic amount of 1,4-diazabicyclo[2.2.2]octane, and a catalytic amount of potassium iodide in 20 mL of pyridine was brought to 50° C. while stirring under nitrogen. After 24 hours, butanediol (0.072 g, 0.8 mmol) diluted in 10 mL of pyridine was added to the reaction mixture using a syringe pump over 8 hours. The solution was then quenched in 200 mL of cold 1N hydrochloric acid. The polymer precipitate is collected by filtration, redissolved in tetrahydrofuran, and precipitated in 100 mL of cold 1N hydrochloric acid. The polymer is then collected by filtration and dried under high vacuum. The polymer was found to have a molecular weight of ˜14,000 g/mol by GPC.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08895691B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-166246f5cd0945e6994ee866b8329084 |
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| Quellennotiz | uspto-grants-2014_11 |
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