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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211184Generated: November 4, 2026

p-Toluenesulfonic acid → 2,6-dichloro-3-methyl-N-[2-(1,3,4-oxadiazol-2-yl)phenyl]benzenamine

https://huagongshe.com/reaction/2211184

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 14951339HCID 14951339—
SolventEthanolHCID 702—
Product2,6-dichloro-3-methyl-N-[2-(1,3,4-oxadiazol-2-yl)phenyl]benzenamineHCID 1937570067%

Reaction Steps

To a room temperature suspension of 2-[(2,6-dichloro-3-methylphenyl)amino]-benzoic acid hydrazide (355.1 mg, 1.15 mmoles) in 6 ml of ethanol is added 2 ml of triethyl orthoformate followed by p-toluenesulfonic acid (20 mg, 0.11 mmoles). After stirring at room temperature overnight, the clear yellow solution is concentrated in vacuo. The residue is subjected to flash chromatography eluting with hexane:ethyl acetate (3:1). Subsequent recrystallization from ethanol yields 244.1 mg (67%) of 2,6-dichloro-3-methyl-N-[2-(1,3,4-oxadiazol-2-yl)phenyl]benzenamine, mp 180°-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05462952
Source datasetuspto-grants-1995_10
ORD IDord-22154f266f6c45058be59d5bc5dab677
Source noteuspto-grants-1995_10