Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288635Generated: November 1, 2026

Sodium Bicarbonate → Ethyl 2-chloro4-fluoro-5-hydrazinobenzoate

https://huagongshe.com/reaction/2288635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
Reactant1,1-Dibromo-3,3,3-trifluoroacetoneHCID 550523—
ReactantEthyl 2-chloro-4-fluoro-5-hydrazinobenzoate hydrochlorideHCID 22508450—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductEthyl 2-chloro4-fluoro-5-hydrazinobenzoateHCID 22508451—

Reaction Steps

To a mixed aqueous solution of 5.3 g (53.5 mmol) of sodium acetate and about 100 ml of water was added under ice cooling 6.6 g (24.3 mmol) of 1,1-dibromo-3,3,3-trifluoroacetone, and the reaction was allowed to proceed at 70° C. for 20 minutes. Then, the reaction mixture was cooled to room temperature. Separately, 5.8 g (21.5 mmol) of crude ethyl 2-chloro-4-fluoro-5-hydrazinobenzoate hydrochloride was dissolved in 30 ml of water, to which 100 ml of diethyl ether was added, and while cooling, the mixture was neutralized by the addition of saturated sodium hydrogen-carbonate solution, followed by washing with saturated sodium chloride solution, which afforded a solution of ethyl 2-chloro-4-fluoro-5-hydrazinobenzoate in diethyl ether. This solution was added to the above reaction mixture, followed by vigorous stirring at room temperature for 2 hours. The ether layer was separated, washed once with 10 ml of saturated sodium chloride solution, and dried with magnesium sulfate. The diethyl ether was distilled out. The residue was dissolved in 50 ml of THF, to which 8.3 g (23.0 mmol) of carbethoxyethylidenetriphenylphosphorane was added, and the mixture was heated under reflux for 2 hours. The THF was distilled out under reduced pressure, and the residue was subjected to silica gel column chromatography, which afforded 3.8 g (10.0 mmol) of compound 1-642. ##STR63##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090753
Source datasetuspto-grants-2000_07
ORD IDord-3c4b3f05d15d489da66b3357a7c93b40
Source noteuspto-grants-2000_07