Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50031Generated: October 26, 2026

Hydrochloric Acid → Ethyl Pyruvate 4-Chloro-3-Fluorophenylhydrazone

https://huagongshe.com/reaction/50031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 2-methylacetoacetateHCID 701—
ReactantPotassium AcetateHCID 517044—
Reactant4-Chloro-3-fluoroanilineHCID 2736511—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductEthyl Pyruvate 4-Chloro-3-FluorophenylhydrazoneHCID 7311574030.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of sodium nitrite (4.76 g, 0.069 mol) in water (6.3 mL) was added dropwise to an ice cooled mixture of 4-chloro-3-fluoroaniline (J. Am. Chem. Soc., 1996, 61, 5130-5133) (10.00 g, 0.069 mol), water (167 mL) and 37% hydrochloric acid (167 mL). After 20 minutes potassium acetate (9.81 g, 0.10 mol) was added, and then a solution of ethyl 2-methylacetoacetate (9.95 g, 0.069 mol), potassium acetate (9.81 g, 0.10 mol) in methanol (67 mL) was dropped while cooling on the ice bad. Reaction was stirred at 0° C. for 3 hours, then extracted with diethyl ether. Organic layer was washed with brine and dried. Removal of the solvent furnished a red oily residue that was treated with ethanol (100 mL) and stirred at room temperature overnight. The solid which formed was filtered a recrystallized from ethanol to give 5.4 g (30%) of title compound, mp 161-163° C. (from ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710068B2
Source datasetuspto-grants-2004_03
ORD IDord-fd12142649ea4bb5af36be8b36b06f39
Source noteuspto-grants-2004_03