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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452573Generated: October 25, 2026

Hydroxyamine hydrochloride → N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-[3-(trifluoromethoxy)phenyl]methanimine

https://huagongshe.com/reaction/452573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant(1-methyl-1H-tetrazol-5-yl)[3-(trifluoromethoxy)phenyl]methanoneHCID 67075092—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductN-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-[3-(trifluoromethoxy)phenyl]methanimineHCID 13633738592%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of (1-methyl-1H-tetrazol-5-yl)[3-(trifluoromethoxy)phenyl]methanone (5.12 g, 16.2 mmol) in dry pyridine (25 mL) was added hydroxylamine hydrochloride (2.81 g, 40.4 mmol). The mixture was stirred at 70° C. for 3 h, then left to stand overnight. After concentration of the reaction mixture in vacuo, the residue was diluted with ethyl acetate (100 mL) and washed with water (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL), the combined organic layers dried (MgSO4), concentrated in vacuo and dissolved in toluene. A crystalline precipitate appeared, which was filtered off to afford N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-[3-(trifluoromethoxy)phenyl]methanimine as a white solid [4.33 g, yield 92%; HPLC/MS:m/z=288 (M+H); log P(HCOOH)=2.37].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492388B2
Source datasetuspto-grants-2013_07
ORD IDord-9a719dbbe32c4adcb817e72b8d34ec10
Source noteuspto-grants-2013_07