Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45276Erstellt: 24. Oktober 2026

4-Methyloxybenzyl chloride → 1-(4-Methoxy-benzyl)-cyclopropanecarbonitrile

https://huagongshe.com/de/reaction/45276

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Methyloxybenzyl chlorideHCID 69993—
EduktCyclopropanecarbonitrileHCID 79637—
Edukt1-(4-methoxy-benzyl)-cyclopropanecarbonitrile Sodium bis(trimethylsilyl)amideHCID 86603547—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(4-Methoxy-benzyl)-cyclopropanecarbonitrileHCID 57456950—

Reaktionsschritte

1-(4-Methoxy-benzyl)-cyclopropanecarbonitrile Sodium bis(trimethylsilyl)amide (2 M in tetrahydrofuran, 37.5 mL, 75.0 mmol) was slowly added to a solution of cyclopropanecarbonitrile (3.35 g, 49.9 mmol) in THF (30 mL) at room temperature. The reaction mixture was stirred for 20 minutes and then a solution 1-chloromethyl-4-methoxy-benzene (7.83 g, 50.0 mmol) in THF was added. The mixture was heated at reflux for 3 hours and then quenched with a saturated aqueous solution of ammonium chloride (50 mL). The separated aqueous layer was extracted three times with ethyl acetate (50 mL). The combined organic layers were washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride, dried over sodium sulfate, filtered, and evaporated to dryness to give crude 1-(4-methoxy-benzyl)-cyclopropanecarbonitrile, which was used directly in the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541453B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-fbc156986c084e01b76995a2830ab6c6
Quellennotizuspto-grants-2013_09