HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39128Erstellt: 24. Oktober 2026
1-Bromo-2-Chloroethane → 1-(2,2-Difluorobenzo[D][1,3]dioxol-5-YL)cyclopropanecarbonitrile
https://huagongshe.com/de/reaction/39128
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2,2-Difluoro-1,3-benzodioxole-5-acetonitrile | HCID 20311384 | — |
| Katalysator | Benzyl triethylammonium chloride | HCID 66133 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(2,2-Difluorobenzo[D][1,3]dioxol-5-YL)cyclopropanecarbonitrile | HCID 57446150 | — |
Reaktionsschritte
Sodium hydroxide (50% aqueous solution, 10 mL) was slowly added to a mixture of crude (2,2-difluoro-benzo[1,3]dioxol-5-yl)-acetonitrile, benzyltriethylammonium chloride (3.00 g, 15.3 mmol), and 1-bromo-2-chloroethane (4.9 g, 38 mmol) at 70° C. The mixture was stirred overnight at 70° C. before the reaction mixture was diluted with water (30 mL) and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and evaporated to dryness to give crude 1-(2,2-difluoro-benzo[1,3]dioxol-5-yl)-cyclopropanecarbonitrile, which was used directly in the next step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524767B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-ef613ac6966f48918c05cb0be902bc62 |
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| Quellennotiz | uspto-grants-2013_09 |
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