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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2296818Erstellt: 25. Oktober 2026

Trichloroacetonitrile → 2,4-Difluorobenzyl trichloroacetimidate

https://huagongshe.com/reaction/2296818

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrichloroacetonitrileHCID 11011—
Edukt2,4-Difluorobenzyl alcoholHCID 91867—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelPotassium HydroxideHCID 14797—
Produkt2,4-Difluorobenzyl trichloroacetimidateHCID 1107707492%

Reaktionsbedingungen

Temperatur-15 °C

Reaktionsschritte

Tetrabutyl ammonium hydrogen sulphate (15 mg) was added to 2,4-difluorobenzylalcohol (1.0 g, 6.94 mmol) in CH2Cl2 (10 ml) and KOH (50%, 10 ml). This mixture was cooled to −15° C. prior to the addition of trichloroacetonitrile (1.2 ml, 8.32 mmol). After 30 min at −15° C. and 3 h at ambient temperature the phases were separated. The aqueous phase was extracted twice with CH2Cl2. The combined organic phases were dried with MgSO4 and reduced to one third. The residue was filtered through celite and concentrated to give the crude 2,4-difluorobenzyl trichloroacetimidate (1.83 g, 92%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06489364B2
Quelldatensatzuspto-grants-2002_12
ORD IDord-28cd121bda794ab8b9cb5eef5712f152
Quellennotizuspto-grants-2002_12