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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276198Generated: October 26, 2026

4-Chlorobenzoyl chloride → 3-(Chloromethyl)-5-(4-chlorophenyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/1276198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantSodium BicarbonateHCID 516892—
Reactant2-chloro-N'-hydroxyethanimidamideHCID 4112252—
SolventAcetoneHCID 180—
Product3-(Chloromethyl)-5-(4-chlorophenyl)-1,2,4-oxadiazoleHCID 12569952—

Reaction Steps

A solution of 2-chloroacetamidoxime (0.5 g) and sodium bicarbonate (0.78 g) in 10 mL of anhydrous acetone was treated with 4-chlorobenzoyl chloride (0.58 mL) at room temperature for 2 hours, concentrated in vacuo, dissolved in water and extracted with ethyl acetate. The organic layers were combined, dried with MgSO4 and concentrated to a semi-solid. This material was redissolved in toluene (50 mL). refluxed under nitrogen for 15 hours, cooled and absorbed on to silica gel. Chromatography using ethyl acetate:hexane (1:9) gave the pure title product as a light yellow solid, mp 79-80° C. Mass spectrum m/e: 228 (M+), 1H NMR (250 MHz, CDCl3) δ 8.1 (d, 2H), 7.5 (d, 2H), 4.7 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166020
Source datasetuspto-grants-2000_12
ORD IDord-8ce304b8faea4ed0b77422013a8ec725
Source noteuspto-grants-2000_12