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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279451Generated: October 29, 2026

Acetic Acid → HCID 54574887, compound

https://huagongshe.com/reaction/279451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethylhydrazineHCID 6061—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantHCID 86584673HCID 86584673—
SolventDiethyl EtherHCID 3283—
ProductHCID 54574887HCID 5457488757.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

Dimethylformamide dimethylacetal (0.53 g, 4.5 mmol) was added to 2-(4-chlorophenoxymethyl)-α-methoxyiminophenylacetamide (0.48 g, 1.5 mmol), and the mixture was stirred under reduced pressure (ca. 40 mmHg) at 60° C. for 0.5 hours. After completion of the reaction, the mixture was concentrated under reduced pressure, and a mixture of methylhydrazine (0.08 g, 1.8 mmol) and acetic acid (3 ml) was added to the residue. The mixture was stirred at 90° C. for 1 hour. After completion of the reaction, ether (150 ml) was added, and the mixture was washed with saturated aqueous sodium bicarbonate solution (100 ml) twice. The ether layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane) and recrystallized from ethyl acetate/n-hexane to give 2-(4-chlorophenoxymethyl)phenyl 1-methyl-1H-1,2,4-triazol-5-yl ketone O-methyloxime (0.31 g, 57.9%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362212B1
Source datasetuspto-grants-2002_03
ORD IDord-2810b4e32e9c4ea8a9b2bbddf49849d1
Source noteuspto-grants-2002_03