Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713038Generated: November 2, 2026

Hydrochloric Acid → Ethyl 2-azido-3-(2-thienyl)propenoate

https://huagongshe.com/reaction/1713038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-ThiophenecarboxaldehydeHCID 7364—
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductEthyl 2-azido-3-(2-thienyl)propenoateHCID 5436214055.5%

Reaction Conditions

Temperature10 °C

Reaction Steps

A solution of thiophene-2-carbaldehyde (650 mg, 5.8 mmol) and ethyl azidoacetate (6.89 grams, 53.4 mmol) in dry toluene (40 ml) was added to a cold (−5° C.) solution of sodium ethoxide (about 53 mmol) in ethanol (60 ml) during a time period of one hour, under nitrogen atmosphere. Stirring was continued for another hour while maintaining the temperature under 10° C. The reaction mixture was then cooled to 0° C. and acidified with HCl 0.1 M. After separation of the phases, the aqueous phase was extracted with ether (3×30 ml), the combined organic phase was dried over Na2SO4 and the organic solvents were evaporated under reduced pressure. The crude product was purified by silica gel flash chromatography to give 718 mg of pure 2-azido-3-thiophen-2-yl-acrylic acid ethyl ester (55% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795255B2
Source datasetuspto-grants-2010_09
ORD IDord-e4d06ddd0a6b4803a97cd2fea85b60c0
Source noteuspto-grants-2010_09