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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564982Generated: October 26, 2026

Ammonium Chloride → Ethyl 3-(4-benzyloxy-2-chlorophenyl)-2-azidopropenoate

https://huagongshe.com/reaction/564982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium ethoxideHCID 2723922—
Reactant4-(Benzyloxy)-2-chlorobenzaldehydeHCID 14034077—
ReactantHCID 86756206HCID 86756206—
SolventEthanolHCID 702—
ProductEthyl 3-(4-benzyloxy-2-chlorophenyl)-2-azidopropenoateHCID 5378316557.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

An ethanol solution, 70 ml, containing 5.40 g (21.9 mmol) of 4-benzyloxy-2-chlorobenzaldehyde and 11.3 g (87.6 mmol) of ethyl azide acetate was gradually added dropwise to 70 ml of an ethanol solution of 5.95 g (87.6 mmol) of sodium ethoxide at −10° C. After stirring at −10° C. for further 5 hours, the reaction temperature was slowly elevated to room temperature. The reaction mixture was poured onto 200 ml of saturated ammonium chloride aqueous solution and the mixture was extracted three times with ethyl acetate. The combined extracts were then washed with saturated ammonium chloride solution and next with saturated sodium chloride solution. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography to give 4.50 g (57.5%) of ethyl 3-(4-benzyloxy-2-chlorophenyl)-2-azidopropenoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169107A
Source datasetuspto-grants-2001_01
ORD IDord-b3ea862860d84752a5790b0c1a26c079
Source noteuspto-grants-2001_01