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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17287Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/17287

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDimethylformamideHCID 6228—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
EduktHydroxyamine hydrochlorideHCID 443297—
Edukt2,2,2-Trichloroacetaldehyde hydrateHCID 20528376—
Edukt3-Fluoro-2-methoxy-5-methylanilineHCID 45122052—
LösungsmittelWaterHCID 962—
Produkt(3-Fluoro-2-methoxy-5-methylphenyl)-2-hydroxyimino-acetamideHCID 8663080510%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737166B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-7aa9800923944b4e93b12b5d5e042baf
Quellennotizuspto-grants-2010_06