HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908096Generated: October 30, 2026
2-Furancarbonyl chloride → HCID 46850915, compound
https://huagongshe.com/reaction/908096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Furancarbonyl chloride | HCID 68242 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178513443 | HCID 178513443 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 46850915 | HCID 46850915 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08017555B2 |
|---|
| Source dataset | uspto-grants-2011_09 |
|---|
| ORD ID | ord-e63aae88c04a496e827c7ccd0fd0d157 |
|---|
| Source note | uspto-grants-2011_09 |
|---|