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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 544921Erstellt: 23. Oktober 2026

Hydrochloric Acid → Ethyl 2-(3-chloro-4-fluoro-phenylhydrazino)propionate

https://huagongshe.com/de/reaction/544921

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthyl 2-methylacetoacetateHCID 701—
Edukt3-Chloro-4-fluoroanilineHCID 9708—
EduktPotassium HydroxideHCID 14797—
EduktSodium AcetateHCID 517045—
EduktSodium NitriteHCID 23668193—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktEthyl 2-(3-chloro-4-fluoro-phenylhydrazino)propionateHCID 6719734534,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of 3-chloro-4-fluoroaniline (10.0 g) in a 6 N aqueous hydrochloric acid solution (35 ml) was cooled to 0° C., and thereto was added dropwise a solution of sodium nitrite (4.80 g) in H2O (6.3 ml). After being stirred at same temperature for 25 minutes, the mixture was added to a solution of ethyl 2-methylacetoacetate (11.0 g), potassium hydroxide (21.2 g) and sodium acetate (21.2 g) in ethyl alcohol (80 ml)-H2O (100 ml) in one portion at 0° C. The resultant mixture was stirred at same temperature for 2 hours, and extracted with diethyl ether. The organic layer was washed with water twice and brine followed by being dried over sodium sulfate. The insoluble materials were filtered off, and the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1-3:1) to give ethyl 2-(3-chloro-4-fluoro-phenylhydrazino)propionate (6.16 g) as a reddish solid. APCI-Mass m/Z 259/261 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07935674B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-0a179adff3f141c2962997c3878a5082
Quellennotizuspto-grants-2011_05