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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57389Generated: October 30, 2026

Diisopropylethylamine → 3-Chloro-N'-hydroxy-4-(trifluoromethoxy)benzimidamide

https://huagongshe.com/reaction/57389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant3-chloro-4-(trifluoromethoxy)benzonitrileHCID 2773846—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product3-Chloro-N'-hydroxy-4-(trifluoromethoxy)benzimidamideHCID 5853878662.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-chloro-4-(trifluoromethoxy)benzonitrile (1.0 g, 4.51 mmol) and hydroxylamine hydrochloride (1.5 eq, 0.47 g, 6.77 mmol) in ethanol (10 ml) was added N-ethyl-N-isopropylpropan-2-amine (1.6 eq, 1.26 ml, 7.22 mmol) and refluxed at 80° C. for 12 hours under N2. Allow to cool to rt. Dilute with EtOAc (25 ml), wash with water (25 ml), brine (25 ml), dry, concentrate in vacuo afforded (Z)-3-chloro-N′-hydroxy-4-(trifluoromethoxy)benzimidamide (0.71 g, 62.1%, white solid). Used crude in the next step. HRMS(B) m/z 254.0070

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-f649e413bff241dc97b169e89c7d8413
Source noteuspto-grants-2016_09