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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908096Generated: October 30, 2026

2-Furancarbonyl chloride → HCID 46850915, compound

https://huagongshe.com/reaction/908096

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarbonyl chlorideHCID 68242—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178513443HCID 178513443—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 46850915HCID 4685091550%

Reaction Steps

To the mixture of 4-chlorophenyl hydroxycarbamimidate (0.5 mmol. 1 eq) and DIEA (1.25 mmol, 2.5 eq) in dioxane was added dropwise furan-2-carbonyl chloride (0.53 mmol, 1.05 eq) at 0-5° C. The mixture was allowed to warm to room temperature and then stirred for 0.5-1 h or until complete as determined by LC-MS analysis of the reaction mixture. The cyclodehydration reaction was run at reflux (115-120° C.) overnight. The mixture was cooled down and solvent was removed in vacuo. The resulting residue was purified by HPLC purification to provide desired 3-(4-Chloro-phenoxy)-5-furan-2-yl-[1,2,4]oxadiazole in a yield of 50% and purity of 99.9%. LC-MS [M+H] 263.3 (C12H7ClN2O3+H, requires 263.65). 1H NMR (DMSO-d6) δ 8.17 (d, 1H, J=1.75), 7.63 (d, 1H, J=3.5), 7.55 (d, 2H, J=8.8), 7.46 (d, 2H, J=8.8), 6.87 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017555B2
Source datasetuspto-grants-2011_09
ORD IDord-e63aae88c04a496e827c7ccd0fd0d157
Source noteuspto-grants-2011_09