Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546796Generated: October 26, 2026

Ethanol → Ethyl 5-chloro-2-(2-trifluoromethylphenyl)pentanimidoate hydrochloride

https://huagongshe.com/reaction/546796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAcetyl chlorideHCID 6367—
Reactant5-Chloro-2-(2-trifluoromethylphenyl)pentanenitrileHCID 66839598—
Solventtert-Butyl methyl etherHCID 15413—
ProductEthyl 5-chloro-2-(2-trifluoromethylphenyl)pentanimidoate hydrochlorideHCID 46854983—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Chloro-2-(2-trifluoromethylphenyl)pentanenitrile (2.0 g, 7.64 mmol) was dissolved in ethanol (5.36 mL, 91.72 mmol) at room temperature under nitrogen atmosphere. Then, the solution was cooled to 0° C. Acetyl chloride (4.34 mL, 61.14 mmol) was added dropwise to the solution, and the reaction mixture was stirred at room temperature for 67 hours. The reaction mixture was cooled to 10° C. Traces of seed crystal of the title compound which was obtained by the method similar to this step and tert-butylmethylether (hereinafter referred to as “MTBE”) (40 mL) were added to the reaction mixture and the reaction mixture was stirred. The solid was collected by filtration, washed with MTBE to obtain the title compound (2.14 g, 81.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935815B2
Source datasetuspto-grants-2011_05
ORD IDord-6a8f3885b2c44ce894efbc4ec6172ff1
Source noteuspto-grants-2011_05