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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Acetic acid, azido-, ethyl ester | HCID 69480 | — |
| Reactant | Potassium ethoxide | HCID 23670592 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-azido-3-(2-thienyl)propenoate | HCID 54362140 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479527B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-080d2bc859cf421d8a886680a13be622 |
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| Source note | uspto-grants-2002_11 |
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