Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant5-(4-nitrophenoxy)furan-2-carbaldehydeHCID 3590045—
SolventEthanolHCID 702—
ProductHCID 86618339HCID 8661833936.6%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795255B2
Source datasetuspto-grants-2010_09
ORD IDord-9280d0a616cd4c23aec22eb6e6ef97a9
Source noteuspto-grants-2010_09