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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1004361Erstellt: 26. Oktober 2026

1,1-Dichloroethane → HCID 54348717, Verbindung

https://huagongshe.com/reaction/1004361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1-DichloroethaneHCID 6365—
EduktThionyl ChlorideHCID 24386—
EduktN-HydroxypropionimidamideHCID 4092053—
EduktHCID 54397424HCID 54397424—
LösungsmittelPyridineHCID 1049—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 54348717HCID 5434871734,5%

Reaktionsschritte

Dichloroethane (5 ml), thionyl chloride (0.65 g, 5.5 mmol) and N,N-dimethylformamide (0.05 ml) were added to 2-(2,5-dimethylphenoxymethyl)-α-methoxyiminophenylacetic acid (1.57 g, 5 mmol), and the mixture was stirred under reflux for 2 hours. After completion of the reaction, the mixture was concentrated under reduced pressure, pyridine (3 ml) and 1-hydroxyimino-1-propylamine (0.88 g, 10 mmol) were added to the residue, and the mixture was stirred under reflux for 0.5 hours. After completion of the reaction, ether (150 ml) was added, and the mixture was washed with 1N hydrochloric acid (150 ml) twice. The ether layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate/n-hexane) and recrystallized from ethyl acetate/n-hexane to give 2-(2,5-dimethylphenoxymethyl)phenyl 3-ethyl-1,2,4-oxadiazol-5-yl ketone O-methyloxime (0.63 g, 34.5%) as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06048885
Quelldatensatzuspto-grants-2000_04
ORD IDord-5be2124b4b6545869780796a70b63879
Quellennotizuspto-grants-2000_04