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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017728Generated: October 30, 2026

2-Thiophenecarboxaldehyde → Ethyl 2-azido-3-(2-thienyl)propenoate

https://huagongshe.com/reaction/1017728

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
ReactantAmmonium ChlorideHCID 25517—
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
ReactantPotassium ethoxideHCID 23670592—
SolventEthanolHCID 702—
ProductEthyl 2-azido-3-(2-thienyl)propenoateHCID 5436214025%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of ethyl azidoacetate (1.38 g) and thiophene-2-carboxaldehyde (1 g) in ethanol (20 ml) was added dropwise to a solution of potassium ethoxide (0.9 g) in ethanol (20 ml) at 0° C. The reaction was stirred for 2 hours at 0° C. and 2 hours at ambient temperature then poured into saturated aqueous ammonium chloride solution (150 ml) and extracted with ether. Combined organic extracts were dried (MgSO4), concentrated in vacuo and the residue purified by column chromatography using isohexane as eluent to give the product as a pale yellow crystalline solid (0.49 g, 25%), NMR d(CDCl3) 1.40 (3H, t), 4.37 (2H, q), 7.08 (2H, m), 7.18 (1H, s), 7.38 (1H, m), 7.52 (1H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479527B1
Source datasetuspto-grants-2002_11
ORD IDord-080d2bc859cf421d8a886680a13be622
Source noteuspto-grants-2002_11