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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355708Generated: October 28, 2026

Ammonium Chloride → Ethyl 3-(3-fluoro-2-methylphenyl)-2-azidopropenoate

https://huagongshe.com/reaction/355708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
ReactantSodium ethoxideHCID 2723922—
Reactant3-Fluoro-2-methylbenzaldehydeHCID 2779235—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(3-fluoro-2-methylphenyl)-2-azidopropenoateHCID 5435915861.5%

Reaction Steps

A solution of sodium ethoxide (11.1 g, 163 mmol) in ethanol (100 ml) was cooled to -45° C. and then a solution of 3-fluoro-2-methylbenzaldehyde (9.00 g, 65.2 mmol) and ethyl azidoacetate (21.0 g, 163 mmol) in tetrahydrofuran (30 ml) were slowly added dropwise therein. The reaction temperature of the mixture was raised from -35° C. to -10° C. over 5 hours and the reaction solution was poured in a cooled aqueous ammonium chloride solution. The resulting mixture was extracted with ethyl acetate and the extract was washed with a saturated ammonium chloride solution and then 5% aqueous sodium chloride solution followed by drying over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was treated with silica gel column chromatography (eluated with ethyl acetate/n-hexane= 3/97) to give 10.0 g of ethyl 3-(3-fluoro-2-methylphenyl)-2-azidopropenoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834454
Source datasetuspto-grants-1998_11
ORD IDord-651823a2bdb44f6ea5cca58774b8ba7a
Source noteuspto-grants-1998_11