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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544921Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 2-methylacetoacetateHCID 701—
Reactant3-Chloro-4-fluoroanilineHCID 9708—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium AcetateHCID 517045—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 2-(3-chloro-4-fluoro-phenylhydrazino)propionateHCID 6719734534.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935674B2
Source datasetuspto-grants-2011_05
ORD IDord-0a179adff3f141c2962997c3878a5082
Source noteuspto-grants-2011_05