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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296818Generated: October 25, 2026

Trichloroacetonitrile → 2,4-Difluorobenzyl trichloroacetimidate

https://huagongshe.com/reaction/2296818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetonitrileHCID 11011—
Reactant2,4-Difluorobenzyl alcoholHCID 91867—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
SolventPotassium HydroxideHCID 14797—
Product2,4-Difluorobenzyl trichloroacetimidateHCID 1107707492%

Reaction Conditions

Temperature-15 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489364B2
Source datasetuspto-grants-2002_12
ORD IDord-28cd121bda794ab8b9cb5eef5712f152
Source noteuspto-grants-2002_12