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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823861Generated: November 3, 2026

4-Chlorobenzoyl chloride → 3-(3-Bromo-thiophen-2-yl)-5-(4-chloro-phenyl)-[1,2,4]-oxadiazole

https://huagongshe.com/reaction/1823861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
Reactant3-Bromo-thiophene-2-amidoximeHCID 86587354—
Product3-(3-Bromo-thiophen-2-yl)-5-(4-chloro-phenyl)-[1,2,4]-oxadiazoleHCID 22147900—

Reaction Steps

The title compound was prepared from 4-chloro-benzoyl chloride (60 μL, 0.47 mmol) and 3-bromo-thiophene-2-amidoxime (102 mg, 0.461 mmol) similar to Example 36c, and yielded 80 mg (51%) of white solid. 1H NMR (CDCl3): 8.15 (dd, J=9.09, 2.06 Hz, 2H), 7.54 (dd, J=8.51, 2.20 Hz, 2H), 7.50 (d, J=5.22 Hz, 1H), 7.18 (d, J=5.22 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041685B2
Source datasetuspto-grants-2006_05
ORD IDord-e980165ce8d14c42ac2a291299a3bcc2
Source noteuspto-grants-2006_05