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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697267Generated: October 31, 2026

Acetic Anhydride → 3-(6-Bromo-naphthalen-2-yl)-5-methyl-[1,2,4]oxadiazole

https://huagongshe.com/reaction/1697267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178513225HCID 178513225—
Solvent2,4,6-TrimethylpyridineHCID 7953—
Product3-(6-Bromo-naphthalen-2-yl)-5-methyl-[1,2,4]oxadiazoleHCID 59534075—

Reaction Steps

6.11 ml acetic anhydride are added to 4.40 g 6-bromo-N-hydroxy-naphthalene-2-carboxamidine in 30 ml 2,4,6-trimethylpyridine. The reaction mixture is stirred for one hour at ambient temperature and then heated to 130° C. for four hours. After the reaction has ended the mixture is evaporated down in vacuo and the flask residue is stirred with ethyl acetate and petroleum ether, suction filtered and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163911B2
Source datasetuspto-grants-2012_04
ORD IDord-5ce417c6628c48d1804740330ea7b28a
Source noteuspto-grants-2012_04