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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263419Generated: November 4, 2026

Triethylamine → HCID 178432700, compound

https://huagongshe.com/reaction/2263419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 59594672HCID 59594672—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178432700HCID 178432700136%

Reaction Conditions

Temperature65 °C

Reaction Steps

3.0 g 2-Chloro-4-{4-methyl-2-[2-(4-trifluoromethyl-phenyl)-ethyl]-oxazol-5-ylmethoxy}-benzonitrile were dissolved in a mixture of 20 ml tetrahydrofuran and 20 ml methanol. 9.91 g hydroxylamine hydrochloride were added followed by the addition of 19.9 ml triethylamine. The reaction mixture was stirred at 65° C. overnight. The solvents were removed in vacuo and the resulting residue poured into water and extracted five times with ethylacetate. The combined organic extracts were washed with brine, dried over MgSO4 and the solvent was evaporated in vacuo to obtain 4.4 g crude 2-chloro-N-hydroxy-4-{4-methyl-2-[2-(4-trifluoromethyl-phenyl)-ethyl]-oxazol-5-ylmethoxy}-benzamidine which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851493B2
Source datasetuspto-grants-2010_12
ORD IDord-1708e11c04174ded8db4f2dc31000cd4
Source noteuspto-grants-2010_12