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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17287Generated: October 25, 2026

Hydrochloric Acid → (3-Fluoro-2-methoxy-5-methylphenyl)-2-hydroxyimino-acetamide

https://huagongshe.com/reaction/17287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant2,2,2-Trichloroacetaldehyde hydrateHCID 20528376—
Reactant3-Fluoro-2-methoxy-5-methylanilineHCID 45122052—
SolventWaterHCID 962—
Product(3-Fluoro-2-methoxy-5-methylphenyl)-2-hydroxyimino-acetamideHCID 8663080510%

Reaction Conditions

Temperature90 °C

Reaction Steps

A N,N-dimethylformamide (30 ml) solution of 3-fluoro-2-methoxy-5-methylaniline (I-26) (4.31 g, 27.8 mmol) and concentrated hydrochloric acid (3.5 ml, 33.4 mmol) were added to a water (60 ml) suspension of trichloroacetaldehyde monohydrate (9.2 g, 55.6 mmol) and anhydrous magnesium sulfate (31.6 g, 222.4 mmol), followed by stirring at 90° C. for 30 minutes, then hydroxylamine hydrochloride (116 g, 166.8 mmol) was added, followed by stirring at the same temperature for 13 hours and a half. After cooling to room temperature, the reaction liquid was filtered through Celite, the filtrate was extracted three times with ethyl acetate, then the organic layer was washed twice with saturated brine, dried over anhydrous magnesium sulfate. After filtration and concentration under reduced pressure, the resulting residue was subjected to column chromatography, and the eluate with chloroform was concentrated under reduced pressure to obtain the entitled compound (596 mg, 10%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737166B2
Source datasetuspto-grants-2010_06
ORD IDord-7aa9800923944b4e93b12b5d5e042baf
Source noteuspto-grants-2010_06