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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402271Generated: October 30, 2026

3,5-Dibromo-4-hydroxybenzoic acid → Ethyl 5-(3,5-dibromo-4-hydroxyphenyl)-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/reaction/2402271

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dibromo-4-hydroxybenzoic acidHCID 76857—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
SolventPyridineHCID 1049—
ProductEthyl 5-(3,5-dibromo-4-hydroxyphenyl)-1,2,4-oxadiazole-3-carboxylateHCID 13613957812.2%

Reaction Steps

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (1.32 g, 10 mmol) was added in one portion to a stirred solution of ethyl 2-amino-2-(hydroxyimino)acetate (1.32 g, 10 mmol) plus 3,5-dibromo-4-hydroxybenzoic acid (2.95 g, 10 mmol) in pyridine (20 mL), the resulting solution was stirred at room temperature for 2 h and then at 90° C. for 5 h. After standing at room temperature overnight the pyridine was evaporated in vacuo and the residue was purified by flash chromatography (silica gel, 10% ethyl acetate/dichloromethane) to give the title compound (0.48 g, 12%) as a colourless solid. 1H NMR δ (ppm) (DMSO-d6): 1.48 (3 H, t), 4.47 (2 H, d), 8.13 (2 H, s), 11.54 (1 H, s, br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796321B2
Source datasetuspto-grants-2014_08
ORD IDord-747478564879444e9c9ce8bd52c427ea
Source noteuspto-grants-2014_08