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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883219Generated: November 1, 2026

Stannous Chloride → 3-(2,6-Dichlorophenyl)-5-(3-aminophenyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/1883219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
ReactantStannous chloride dihydrateHCID 61436—
Reactant3-(2,6-Dichlorophenyl)-5-(3-nitrophenyl)-1,2,4-oxadiazoleHCID 11359608—
SolventEthyl AcetateHCID 8857—
Product3-(2,6-Dichlorophenyl)-5-(3-aminophenyl)-1,2,4-oxadiazoleHCID 11460935—

Reaction Steps

The nitro oxadiazole prepared in Step 1 (200 mg) was dissolved in ethyl acetate (20 mL) and tin (II) chloride dihydrate (162 mg, 1.2 molar equivalent) was added. The mixture was stirred at room temperature for 1 h. An additional 1.2 molar equivalents of tin (II) chloride was added. After a further 4 h at room temperature, the reaction mixture was diluted with ethyl acetate and washed three times with water. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the desired 3-(2,6-dichlorophenyl)-5-(3-aminophenyl)-1,2,4-oxadiazole as a white solid in quantitative yield. NMR (300 MHz, DMSO-d6): 7.70 (m, 3H), 7.36 (s, 1H), 7.24 (d, 2H), 6.91 (m, 1H), 5.57 ppm (broad s, 2H). LC-MS tr=33.1 min (Method W) MH+=307

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759538B2
Source datasetuspto-grants-2004_07
ORD IDord-634ea17398fb4937a9657f328f9f53a5
Source noteuspto-grants-2004_07