HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713043Generated: November 2, 2026
Acetic acid, azido-, ethyl ester → HCID 86618339, compound
https://huagongshe.com/reaction/1713043
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic acid, azido-, ethyl ester | HCID 69480 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 5-(4-nitrophenoxy)furan-2-carbaldehyde | HCID 3590045 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86618339 | HCID 86618339 | 36.6% |
Reaction Steps
Absolute ethanol (20 ml) was added to 5-(4-nitro-phenoxy)-furan-2-carbaldehyde (275 mg, 1.18 mmol) and the mixture was heated to 70° C. until a limpid solution was obtained. Azido-acetic acid ethyl ester (1.827 grams, 14.2 mmol) and DBU (286.9 mg, 1.89 mmol) were then added and the mixture was heated at 70° C. for one and a half hours. The solvent was thereafter removed under reduced pressure and a solution of HCl 0.1 M (50 ml) and ethyl acetate (20 ml) were added. After separation of the phases the aqueous phase was extracted with ethyl acetate (2×20 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 148.5 mg of pure 2-azido-3-(5-(4-nitrophenoxy)-furan-2-yl)-acrylic acid ethyl ester (36.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795255B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-9280d0a616cd4c23aec22eb6e6ef97a9 |
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| Source note | uspto-grants-2010_09 |
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