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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45278Erstellt: 24. Oktober 2026

1-Bromo-2-Chloroethane → 1-(2,2-Difluorobenzo[D][1,3]dioxol-5-YL)cyclopropanecarbonitrile

https://huagongshe.com/de/reaction/45278

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-2-ChloroethaneHCID 7849—
Edukt2,2-Difluoro-1,3-benzodioxole-5-acetonitrileHCID 20311384—
Edukt1-(2,2-Difluoro-benzo[1,3]dioxol-5-yl)-cyclopropanecarbonitrile Sodium hydroxideHCID 67315152—
KatalysatorBenzyl triethylammonium chlorideHCID 66133—
LösungsmittelWaterHCID 962—
Produkt1-(2,2-Difluorobenzo[D][1,3]dioxol-5-YL)cyclopropanecarbonitrileHCID 57446150—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

1-(2,2-Difluoro-benzo[1,3]dioxol-5-yl)-cyclopropanecarbonitrile 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. and 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541453B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-7ed85289fe0e4e46950710b1bf82c8b3
Quellennotizuspto-grants-2013_09